craigslist | science/biotech jobs in boston

Staff Geologist (Boston / Cape Cod)

2009-12-21T14:54:38-05:00

Engineering Firm seeks qualified candidate for Staff Geologist Position.

Minimum Credentials: B.S. in Geology, Engineering, or Environmental/Earth Sciences.

Minimum Qualifications: 2 � 5 years of experience in the environmental industry with direct experience and oversight of rotosonic drilling rig operations, soil and water sampling during drilling, soil classification, and monitoring well installation. Soil classification/lithologic characterization is to be performed by a geologist or hydrogeologist appropriately trained and experienced in sample characterization.

Must have direct experience in rotosonic drill rig operations, performing soil logging using the USCS, and collecting soil and groundwater samples following EPA protocols.

Must be current in 40 HAZWOPER training.

Proficient verbal and written communication skills.

Self Motivated

Trustworthy and a Team Player

Compensation Package: Competitive salary and benefits based on qualifications.

Part Time Research Associate (Cambridge, MA)

2009-12-21T13:25:28-05:00

Candidate will learn activities / tasks associated with role in a research setting
Will work / cooperate with colleagues on various assays.
Typically has up to two years of experience.

SKILLS

Understands and effectively conducts laboratory experiments.
Experience with molecular, biochemical or immunoassays
Contributes to written presentations.
Participates in experimental design.
Conducts defined work assignments.

EDUCATION

Must have a BS or MS in Biology, Biochemistry, Immunology or related field with 1 - 2 years research experience

Please note this is a Part Time opening. Candidates will be expected to work a full 8 hour day 3 days a week

Candidates MUST live local and be a US Citizen or Permanent Resident Green Card Holder

Please submit resumes to jobs@cwsciences.com and refer to job #CL-2145

Commonwealth Sciences, Inc.
http://www.cwsciences.com

Environmental Lab Tech (Salem, MA)

2009-12-20T16:42:34-05:00

Our environmental testing laboratory is currently seeking a lab technician. The qualified individual must be responsible, organized and self-motivated.
This position involves the analysis of soil and water by GC, GC-MS and ICP. Analyses are performed according to EPA methodology.
A successful candidate must possess excellent problem solving and trouble shooting skills

Position Requirements
� Minimum 24 Credit hours in Chemistry � degree in chemistry or closely related field preferable
� Familiarity with GC, GC-MS and ICP a plus
� Must be able to work independently
� 30+ hours per week
� Compensation based on experience

We would be consider training an exceptional candidate.

Research Communications Associate Part-time (Watertown, MA)

2009-12-18T19:16:45-05:00

Position summary:

The National Brain Tumor Society is a progressive and thriving nationwide non-profit organization based in San Francisco, CA and Watertown, MA. The Research Communications Associate reports to the Chief Scientific Officer and is responsible for communicating the Society�s research agenda and programs. This may include organizing of research meetings and conferences, tracking and conveying brain tumor scientific progress in the field, preparing research communications to NBTS constituents including donors, and interacting with scientists and research business leaders in academics and industry. This is a part-time position, 24 hours per week.

Primary Responsibilities:

� In collaboration with the research team, stay informed of brain tumor scientific research developments in both the academics and bio/pharmaceutical arenas. These developments include all areas that have potential to effect brain tumor research, such as other cancers and enabling technologies. Collaborate with the Communications team to communicate the information and updates internally and externally.
� Participate with CSO and research staff in development of themes for research workshops/meetings on critical brain tumor research issues that bring together thought leaders in order to help generate forward thinking on those issues. Responsible for project management of research workshops/meetings in collaboration with NBTS Communications and events planning staff.
� Contribute to the development and preparation of research related communications content and materials for NBTS publications, website and other communications media for internal use and to the brain tumor community.
� Conduct analyses of effectiveness of NBTS programs and research grant investments and write associated reports as needed.
� Support the CSO in managing departmental work as needed.

Job Qualifications:

� Background in biological sciences (biochemistry, cell biology, molecular biology, oncology, or related fields) preferably at the Masters Degree level.
� Minimum of three years experience working in a biological sciences research arena.
� Adept at comprehending, synthesizing and communicating complex biological cellular/molecular/biochemical processes to lay and scientific audiences.
� Ability and willingness to learn about brain tumor laboratory/clinical science and research.
� Demonstrated program/project planning, execution and management experience and expertise.
� Ability to work both independently with initiative and as part of a team.
� Strong written/oral communications and interpersonal skills.

To apply: Please send a resume and cover letter (required) to the Director of Human Resources at employment@braintumor.org. National Brain Tumor Society is an equal opportunity employer. Due to the volume of applications, only those who are selected for an interview will be contacted.

Molecular Biologist (Cambridge)

2009-12-18T16:59:02-05:00

Molecular Biology Lab Technologist

DNA extraction from human samples
DNA Sequencing
Microarray analysis
Troubleshooting and validating assays
Timely delivery of clinical reference lab results to clients, which will include clinicians and collaborative partners
Evaluate test results for completeness, accuracy and quality
Follow and operate in accordance with requirements, policies and procedures
BS degree and 2+ years of molecular biology experience.

MUST BE LOCAL

MUST BE ELIGIBLE TO WORK IN THE US

Analytical Chemist (Lexington, KY)

2009-12-18T16:53:26-05:00

Job Description: As an Analytical Chemist you will perform chemical and physical analysis for raw materials, API, and drug products. Responsibilities include analytical method verifications, transfers, development and validations in support of early research as well as late-stage development projects. You must have recent industry related experience with specific focus on HPLC as well as a strong understanding of GMP�s. The successful candidate will be able to work well independently as well as part of a dynamic team.

Requirements: BS or MS in Chemistry or related field and at least 2 years biotech or pharmaceutical industry experience in an analytical laboratory. If you do not have industry experience, please do not apply for this position.

Part Time Research Asst/Administrator/Editor @Harvard Affiliated Group (Cambridge)

2009-12-18T16:50:35-05:00

While the job requires a bit of ordinary administrative work (about 5 hours a week), most of the work requires a very high level of skill in helping write research papers and grants, editing scientific content for the group's web-site, and editing a web-journal on mathematical biology. Such a job would be suitable for an individual who was in the world of work or academia, but has taken a step away (i.e. is raising a family, or is temporarily in the greater Boston area with a spouse who is in training), wants to work part time, but still wants to do something interesting and demanding. Most of the work can be done from home. The hours are completely flexible, involves interesting people and is interesting intrinsically. The work requires quite high level of skill, especially in writing. A bit of scientific knowledge would be useful.

MGH/Harvard/MIT Health Systems Research for Undergrad Winter Recess+ (Cambridge)

2009-12-18T16:47:50-05:00

Medical Systems Research Position For An Undergraduate During Winter Recess
The work concerns the creation of a system for tracking patients with signs suggestive of breast cancer, and the analysis of how patients and information move through the medical system.
The work can be begun full time over the Winter Recess, with the opportunity to continue part time during the spring semester, and full time starting in June.
The program is a collaborative project between individuals at the Massachusetts General Hospital, Harvard, and MIT, and is located in an MGH facility next to MIT in Cambridge.
Reply by email with CV or resume

Computational Biologist (Cambridge, MA)

2009-12-18T14:52:18-05:00

COMPUTATIONAL BIOLOGIST, Broad Institute-Genome Sequencing and Analysis Group, Medical Population Genetics Program to conceive and develop algorithms and analysis approaches to solve the key challenges for emerging DNA sequencing technologies, instantiate these ideas in usable software tools, and apply these tools to flagship Program projects like 1000 Genomes with revolutionary implications in human medical genetics. Will join a lively team and wider community of computational biologists, medical geneticists, and software engineers dedicated to creating a general-purpose toolkit for applying next-generation DNA sequencing to medical genetics.

Characteristic duties include: applying computational techniques and biological domain knowledge to design and implement analysis tools to solve complex computational and mathematical problems; envisioning new algorithms and new approaches to data analysis; rapidly prototyping these ideas, validating their value on novel data sets, and implementing and optimizing successful algorithms for use by the broader community; working collaboratively with other scientists on computational research in a fast-paced environment; and preparing written reports and presentations for internal use and publication. Must enable the research of other program scientists though excellent communication, teamwork, and a focus on creating usable and accessible research software tools.

REQUIREMENTS: exceptionally deep computational and analytic abilities demonstrated by a top-tier Ph.D. in the life sciences with significant programming and algorithm development experience or a top-tier Ph.D. in math, physics, computer science, or related field and familiarity with biological research problems. Must have track record of high-quality computational research. Must possess excellent general computational and programming skills; familiarity with Java (or C/C++), Python (or Perl), and analysis tools like MATLAB and/or R. Prior biological research experience a plus. Must be capable of understanding and translating high-level scientific goals into concrete computational approaches. Excellent oral and written English communication skills required. Must be capable of working in an interactive team environment while conducting self-directed research within broader goals set by group.

The Broad Institute was launched to pioneer a new model of collaborative biomedical science that would transform medicine. To accomplish these goals, we have built an amazing team of talented Broadies who work together to realize this transformation.

We are always looking for new Broadies to join our team and help us tackle important problems at the cutting edge of science.

The Broad community

The Broad community includes professional scientists from many disciplines, administrative staff, and students. We seek to cultivate an interdisciplinary, goal-oriented work environment that unleashes scientific creativity and empowers our people to pursue ambitious and critical projects.

Our work transcends traditional academic boundaries, giving Broad employees and affiliates access to an unparalleled biomedical research community across the Harvard and MIT communities and beyond.

Benefits of working at Broad

The Broad Institute is committed to providing its employees with a competitive compensation and benefits package. We recognize the need for our employees to have a balance between work and personal life. To that end, our benefit plans and options reflect our desire to promote an environment that supports the health, diversity, and general wellbeing of our employees.

All Broadies also have access to world-class research and state of the art technology and are fully supported in their professional development, pushing the envelope for further growth.

The Broad Benefits Program includes:

- Medical: choice from 2 HMOs and 1 PPO. Broad pays 80% of premiums.
- Dental: 1 enriched plan. Broad pays 80% of the premiums.
- Basic Life Insurance, Accidental Death & Dismemberment, Business Travel paid in full by Broad
- Supplemental Life Insurance choices for yourself, your spouse and children
- Short-Term and Long-Term Disability paid in full by Broad
- Flexible Spending Accounts, Health care, Dependent care, and Parking
- 401(K) Plan w/ 6% Employer Match, and Annual Contribution (discretionary but targeted at 4% for 2010)
- 4 Weeks of Vacation after 1 Year
- Tuition Reimbursement - 1 class each semester at MIT/Harvard paid in full (2 per year maximum)
- Identity Theft Prevention and Insurance paid in full by Broad
- Estate Planning - free will preparation
- Adoption Assistance
- Employee Assistance Program (EAP)
- MBTA Commuter & Transportation Subsidies (50% up to the federal maximum)
- Subsidized onsite parking, occasional parking, van pool, and car pool programs available
- Parents in a Pinch Back Up Child Care
- Credit Union
- Discounted Fitness and Gym memberships
- Pet Insurance
- Group Home & Auto Insurance
- Group Legal Program

The Broad Institute is an equal opportunity employer.

If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id=845407-1857-3739

Operations Manager (Boston)

2009-12-18T14:26:51-05:00

Operations Manager

Brigham and Women's Hospital is accepting applications for an Operations Manager for its Cyclotron and Radiochemistry Program. The successful candidate will be responsible for managing the production of clinical and research radiotracers, animal imaging, and research activities in compliance with Department and hospital policies & procedures, and guidelines issued by the FDA, Mass Department of Public Health, Mass Board of Pharmacy and other agencies as appropriate. The incumbent will be responsible for the operational management of the Program. Responsibilities include the program�s operating and capital budgets, the facilitation of research operations and activities of the faculty, overseeing the manufacture of PET radioisotopes and the distribution of PET and SPECT-related radio-diagnostic and radio-therapeutic agents. Ensures that the cyclotron, its targets and syntheses systems, hot cells, clean rooms, animal scanners, analytical instruments, environmental and safety controls are properly operated and maintained. The manager will facilitate resource scheduling and utilization, and will collaborate with the core�s experts in research activities for the development of new targets, syntheses, and handling of technologies. Qualified applicants should send their Curriculum Vitae, cover letter, and 2 references to: Victor H Gerbaudo, Ph.D., Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Brigham and Women�s Hospital, 75 Francis Street, Boston, MA 02115. E-mail: vgerbaudo@partners.org; Fax: 617-582-6056. Brigham and Women's Hospital/Harvard Medical School is an affirmative action/equal opportunity employer and educator.

Cyclotron and Radiochemistry Program

Experience in training and supervising staff involved in PET radiotracer production, with excellent human and communications skills are requisite. The position requires a Masters degree or equivalent experience (minimum of 5 years) in a relevant scientific discipline (e.g., PET Radiopharmacist; Engineer with accelerator technology experience; PET Physicist). Must have formal management training, and a minimum of five years of experience leading a PET radiopharmaceutical operation.

PhD or MD editor for online video journal (Cambridge/Somerville - Davis Square)

2009-12-18T11:30:32-05:00

Journal of Visualized Experiments (JoVE, www.jove.com), is a young scientific publishing company developing a new type of biological research journal using video online. We are looking for energetic individuals to grow the journal content in specific areas: Medicine, Neuroscience, Immunology, Bioengineering and Plant Biology. The responsibilities will include developing and recruiting the content from academic labs.

Requirements:
- Ph.D. degree with a good knowledge in one of the areas: Neuroscience, Immunology, Bioengineering or Plant Biology.
- ability to effectively communicate with people, by phone and email. Previous experience in marketing or sales or fundraising is a plus.
- must be organized, energetic and independent.

We are looking for people who will start working part-time and become full-time if successful.

JoVE is a young dynamic start-up aiming to increase productivity in biological and biomedical research employing novel video-based publication of research methods. Our office is very close to the Davis Square Red Line T station.

Please send your resume and a short description why you are suitable to this position.

TECHNICAL RES ASST I I / 40 HOURS / DAYS - BWH (2197173) (Boston-On Campus/Longwood Area)

2009-12-18T10:45:13-05:00

Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ OVERVIEW STATEMENT:
Experienced Technical Assistant, working independently under general supervision of the Principal Investigator, predominantly working with primary tissues and cell lines from human breast, lung, and ovary. Primary responsibility is establishment and propagation of tissue culture (TC) cells, preparing and maintaining TC stocks and inventories. Analysis of tissue cultured cells using basic cell biology and molecular biology techniques. Injection of tumor cells into laboratory mice, monitoring of tumor growth and necropsy examination of mice.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Semi-independently designs, plans, organizes, and conducts tissue culture experiments in order to optimize culture conditions for different primary human cells (normal and malignant) from epithelium of organs such as breast, ovary, prostate, lung, peritoneum, etc. A typical experiment would minimally require monitoring influence of cytokines on growth curves multiple cells.
2. Analyzes gene expression; protein levels (Western), RNA levels (Northern blots, RT-PCR), and DNA (Southern blots) in these cells.
3. Transfects and infects ectopic genes into cells using retro and lentiviral vectors in order to study the effect of these genes on tumor formation.
4. Implants tumorigenic cells into laboratory mice to create xenograft tumors, monitors tumor growth twice a week, euthanizes tumor bearing mice, explants and examines xenograft tumors. Processes explanted tissue in order to submit for histopathological examination.
5. Collects, records, analyzes data using advanced statistical techniques and helps in preparation of reports of completed projects for publication in technical journals, presentations at professional field meetings/conferences, and for use in further applied or theoretical research activities.
6. Labels tissue cultured cells with antibodies for FACS analysis and magnetic cell sorting.
7. Maintains lab supply and reagent inventories and orders supplies and minor equipment.
8. Coordinates lab compliance with institutional policies and procedures in the areas of safety, environmental and infection control.
9. Assists in the orientation and training of new personnel.
10. Perform all other duties and responsibilities as directed.

QUALIFICATIONS:
Minimum Bachelor of Science in Biology, MS in a Biological Science preferred.
Minimum two (2) years of laboratory experience, with at least one (1) year of full-time employment at a research laboratory in an academic institution (preferred), or industry.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
Independent trouble shooting skills and attention to detail is essential.
Sound analytical and organizational skills with computer literacy required.
Must be able to conduct in vivo experiments, work with mice and human tissues/blood.
Excellent oral and written communication ability with good interpersonal skills required.
Ability to learn new methods and skills desirable.

WORKING CONDITIONS:
Basic science laboratory environment.
Exposure to laboratory reagents, chemicals, radioactive molecules, replication deficient viral vectors and mouse and human tissues under controlled conditions. Minimal risk when established protocols are followed.

SUPERVISORY RESPONSIBILITY:

Will participate in the orientation of new research staff.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2197173

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

RESEARCH ASSISTANT II -post-graduate training- (2196462) ( Boston-On Campus/Longwood Area )

2009-12-18T10:30:32-05:00

Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

Department Overview
Research Assistant II position, working very independently and under general supervision from a Principal Investigator or manager, available immediately to study the relationship between surgeon and obstetrician fatigue and operating room safety. The Research Assistant II will play a key role helping to design and carry out a clinical research project. The Research Assistant II will assist in study design, conduct direct observations in the OR, review charts, and assist with analyses. A medical degree and post-graduate training in surgery or obstetrics required, but a license to practice medicine not necessary. Clinical research experience a plus. May be responsible for the following activities: aids in study design; makes independent judgment, in concert with the Principal Investigator, develops and implements strategies for recruiting, collecting and organizing subject data; conducts direct observations in the OR; reviews charts; scheduling subjects for study visits, maintains and updates data generated by the study and oversees the work of more entry level staff.

Responsibilities
1. Performs surgical observations in the operating room along with other observation team members.
2. Reviews medical records.
3. Develops, organizes, updates and/or maintains human research subject information database for study. Required to input data, and present weekly reports.
4. In conjunction with the Principal Investigator/Project Leader, develops and prepares research protocols including, design, data collection systems, internal review board approval (IRB) applications/amendments and annual reports.
5. Assist the PI and Project Leader with preparation for presentations and written published article.
6. Oversee the work of more entry level staff.
7. Performs all others duties, as required.

QUALIFICATIONS:
1. MD (or equivalent) and post-graduate training in surgery and/or obstetrics (medical license not required)

2. Working knowledge and proficiency with the following computer software: word processing, spreadsheets, PowerPoint and email

3. Research experience a plus.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
1. Ability to work independently.
2. Competence (at a resident-physician level or higher) in obstetrics / gynecology or surgery
3. Excellent interpersonal skills are required for working with the study participants.
4. Good oral and written communication skills.
5. Knowledge of clinical research protocols
6. Knowledge of computer programs, database, etc.
7. Excellent organizational skills and ability to prioritize a variety of tasks.
8. Careful attention to detail.
9. Ability to demonstrate professionalism and respect for subject rights and individual needs.

WORKING CONDITIONS:
The work takes place in a busy academic/research office setting.
Potential exposure through contact with biological specimens.

SUPERVISORY RESPONSIBILITY:
Responsible for supervising surgical observations in the operating room.

Shift
Rotating Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2196462

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

Software Developer I for science education company (Missoula,MT)

2009-12-18T10:23:05-05:00

SimBiotic Software is a leading developer of cutting edge software for teaching biology. SimBiotic is looking for an entry level programmer to support several new projects. See description of job on our website.

Note that this job is in Missoula, MT. However, we also have an office in Boston, and interviews can be conducted in Boston. If you have the skills described in the job ad and have always dreamed of moving to the rockies, this job is for you.

Full-time
Start Date: ASAP
Only candidates in Montana or in the greater Boston area willing to move to Montana will be considered

TECH RESEARCH ASST I / 40 HOURS / DAYS - BWH NEUROLOGY (2195289) (Boston-On Campus/Longwood Area)

2009-12-18T10:12:59-05:00

Technical Marketing and Regional Sales Manager (East Coast)

2009-12-17T17:19:44-05:00

RheoSense is a manufacturer of innovative viscometers based on proprietary chip technology in San Ramon, California. We are looking for a visionary and energetic technical expert in rheology or viscometry who is highly motivated to be a big player in areas of technical sales covering East region and marketing. This is a position with potential for growth and exciting reward.

Key responsibilities of the positions include, but are not limited to:
� Sales and marketing operation
� Coordinate and perform customer demonstrations, ensuring all customer needs are met.
� Coordinate and lead trade show exhibitions
� Develop and execute plans for product promotion through press-releases, release of white papers, or application notes
� Facilitate and/or drive customer-issue resolution through technical leaderships and organizational leadership
� Provide technical assistance directly or indirectly to customers, build and maintain strong customer relationships through excellence in service
� Communicate customer perspectives with technical staffs in order to guide technical trends.
� Coordinate and establish global distribution channels
� Write internal and external reports, documenting customer demonstration and unmet needs
� Meet regular sales targets

Qualifications:
� MS in engineering or higher degree is preferred
� Understanding of viscometers and applications
� Two to five years experience in technical sales or strong desire to be one
� Exceptional interpersonal and communication skills
� Ability to win customers
� Entrepreneurial mindset, roll up sleeves and pitch in when needed
� High level of travel

We offer excellent compensation package plus sales incentives. All applicants must send a cover letter with resume to hr@rheosense.com, or fax to (925) 866-3804.

Research Associate: In Vivo Pharmacology (Cambridge, MA)

2009-12-17T16:54:55-05:00

Job Title: Scientific Associate - In Vivo Pharmacology - Ophthalmology

Duties:
Scientist responsible for carrying out in vivo and in vitro pharmacology and pharmacokinetic experiments in animal models of eye diseases. He/she will be accountable for evaluating test compounds in these models. The candidate should have experience and expertise in in vivo pharmacology and animal surgery.

Skills:
The candidate will analyze scientific results, provide oral and written reports, and remain current with regard to literature reports and technological developments.

Education:
BS or MS degree in physiology, pharmacology, cellular biology, or related discipline; minimum of 1 year experience, preferably in the pharmaceutical or biopharmaceutical industry; broad scientific foundation, strong work ethic, excellent oral and written communication, and ability to function in an interdisciplinary team setting are essential.

Research Assistant (Boston)

2009-12-17T15:43:14-05:00

Position available for a Research Technician / Research Assistant at Harvard
Medical School, in a molecular biology laboratory. The lab studies gene
regulatory events that control metabolism in the cardiovascular system, with
a focus on mitochondria and the relationship between metabolism and blood
vessels (e.g. angiogenesis). Work will involve a range of molecular
techniques, including DNA handling, quantitative real-time PCR,
protein-based assays, and metabolic assays, as well as frequent use of mouse
models. The setting is highly stimulating, in a world-class research
environment, with numerous chances for attending seminars and other learning
opportunities. Independence and initiative will be fostered. Compensation
is competitive with equivalent positions in the area, including full range
of benefits. Applicant must have a BA/BS (or higher) in a biological field;
must be willing to commit two years to the laboratory; and must be willing
to work with mice. Please send CV, brief cover letter, and 3 contacts for
references.

RESEARCH COORDINATOR - Biomedical Engineering (Medford, Massachusetts, 02155 )

2009-12-17T15:05:30-05:00

This position is a 2-year limited appointment with the possibility of an extension based on continued grant funding. As this position is grant-funded it is not eligible for severance pay.

The Biomedical Engineering Department is a multi-disciplinary department that offers comprehensive research opportunities for those interested in the field, with significant emphasis on areas such as biomaterials, drug delivery, and tissue engineering. A research initiative on the development of platform technologies for the controlled, sustained release of pharmaceuticals has been funded in the Department of Biomedical Engineering at Tufts. This particular initiative focuses on biomaterials preparation, characterization and optimization for biocompatibility in vitro and in vivo for a sustained drug delivery system.

The key responsibilities for the Research Coordinator include but are not limited to: collecting, organizing, analyzing, and reporting scientific data, as well as aiding in the administrative duties of the lab. The Research Coordinator will be responsible for laboratory activities, including supply and maintenance of the labs, coordinating group meetings, and carrying out laboratory work for materials preparation and other experiments as needed. The Research Coordinator must be self-motivated and have superb communication/organizational skills. She/he must be able to collect, organize, and report scientific data with proficiency.

Basic Requirements:

Bachelor of Science in scientific or engineering discipline
0-2 years of lab experience
Proficiency in Microsoft Office

Preferred Qualifications:The ideal candidate will have 2+ years of lab experience (industry preferred). Previous experience with drug delivery/formulation product development is desirable. Experience with the use and maintenance of one or more analytical methods (e.g., HPLC/MS, LS, rheology, microscopy), biochemical assays (e.g., SDS/PAGE, ELISA) and/or liquid-handling robotic devices is also a plus.

Tufts University is an AA/EOE employer and actively seeks candidates from diverse backgrounds.

Apply Online

Research Assistant (Boston)

2009-12-17T14:25:35-05:00

Joslin Diabetes Center

Only a multi-disciplinary approach, such as that found in the Research Division at Joslin Diabetes Center, can fully explore the most promising pathways to prevent, treat and cure type 1 and type 2 diabetes and their complications. For diabetes is not a single disease, but rather a complex problem caused by multiple genes and environmental factors that call for scientists to attack it from many perspectives.

Uniquely Joslin
Our investigators, who engage in both basic and clinical research across the sections into which the Research Division is organized, are advancing science at an unusually fast pace due to Joslin�s unique environment. What sets us apart is our critical mass of researchers whose focus is diabetes and our one-of-a-kind resources that facilitate rapid scientific progress.

The main focus of our lab is on the investigation of the development of insulin resistance using cell and small animal models. The primary project of the Research Assistant is to assist in the analysis of insulin signaling in cells and in transgenic and knock-out mouse models.

Specific tasks include maintaining cell lines in culture, maintaining the colony of transgenic and knock-out mice (including numbering, tailing, genotyping, breeding and weighing mice, measuring food intake, physiological characterization of mice including blood sampling). Bench laboratory work will include PCR, Western, Southern and Northern blotting, enzyme assays and analysis of cell culture and mouse blood samples. The Research Assistant will coordinate experiments with the rest of the group in the lab and will be responsible for some lab duties. The Research Assistant should be flexible to drive to an off-site Animal Facility using the Joslin Van at least twice a week.

Qualifications include:
� B.S. in biochemistry, biology, molecular biology or related field.
� Some experience with biochemical, molecular and cellular studies.
� Previous experience with small animal (mice and rats) work is preferred but not essential.
� Valid MA driver�s license with clear driving record.

Interested applicants should apply on line at www.joslin.org
Apply to Job 1942: http://jobs-joslin.icims.com/jobs/1942/job

Joslin Diabetes Center is an Equal Opportunity Employer M/F/D/V

Project Scientist (Burlington, MA)

2009-12-17T12:17:41-05:00

Project Scientist� Job # 28058

Position Description
EBI Consulting is a full-service Environmental Health and Safety (EH&S) management consulting company with 20 years of experience successfully assisting telecommunications, wireless, and related program management companies with network expansions and build-out programs. We are seeking a full-time Project Scientist to conduct Phase I Environmental Site Assessment reports and National Environmental Policy Act (NEPA) reports. This position will require you to perform field inspections of various property types, primarily sites under consideration for telecommunications installations. You will perform independent research of local, state, and federal resources in compiling the information required for Phase I ESAs, and NEPA Screening Reports. Technical report writing is required. The position typically involves approximately 50% field time and 50% office time.

Experience required
Prior experience with Phase I Environmental Site Assessments and NEPA Reports conducted for wireless carriers, tower companies, acquisition firms, or lenders.
� A professional science degree in environmental science, ecology, biology, geology, engineering, or related field, and at least two years professional experience in NEPA consulting and/or due diligence.
� An understanding of and experience with NEPA reviews for proposed construction projects, including evaluating impacts to floodplains, wetlands, endangered species habitats, and historic properties
� Excellent report writing skills, computer and internet skills
� Excellent communication and management skills
� Excellent time management and organizational skills. This position will require you to simultaneously manage electronic deliverables on many ongoing projects.
� Ability to complete assignments on-time and within budget
� Ability to travel on short notice (1 week or less). This position will require travel primarily throughout the Western Region as well as occasional trips throughout the US in an effort to support national needs. All related travel expenses are reimbursed.
� LBP and ACBM Certification a PLUS.

Education Requirements
BA or BS in Environmental Science, Ecology, Biology, Geology, Engineering or related fields

Company Overview
EBI Consulting was founded in 1989 with the purpose of creating value for our clients by utilizing innovative applications of engineering assessments, environmental health and safety (EH&S) management, and due diligence techniques. EBI Consulting is know for the high quality of our product, the professionalism and business expertise of our consultants, our responsiveness, and the personalized nature of our services. EBI Utilizes, and is constantly improving upon, state of the art technology and communications to expedite the delivery of our services. Nationwide offices help to ensure exceptional, efficient, cost-effective and expedited services.

EBI has grown and been profitable for more than 20 years, has no indebtedness to banks or outside investors, and is currently investing in new technology and personnel with the primary objective of improving profitability for its clients. EBI�s people have years of successful business and technical management experience with multi-national companies including W.R. Grace & Company, Earth Tech, Dow Chemical�s Rohm & Haas/Shipley Company, and Stone & Webster Engineering. EBI�s personnel have advanced business management and technical degrees including chemistry, biology, geology, geophysics, and structural, civil, electrical and environmental engineering and certified industrial hygiene.

For more information about EBI and open positions please visit our website at www.ebiconsulting.com.

Plans and Expectations for Future Growth
After adjusting to the 2007-2008 changes in economic conditional, EBI has developed and followed an aggressive plan to develop new services and business lines, acquire new clients, and invest in existing lines of business that have the potential for significant growth. Our goal and strategic plan call for EBI to grow revenues from $30M to over $50M in three years.

What the Successful Candidate should anticipate
We expect the successful candidate would work with our team to help EBI realize our goals while at the same time, the successful candidate will realize personal, professional and financial growth.

Benefits
EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities.
EOE M/W/D/V

Submittal
Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com. You must include the following information:

1. Reference job #, job title and resource
2. Brief summary of past related experience (highlight your experience as it relates to our need & industry);
3. List of your education credentials and professional registrations
4. Salary history

We look forward to hearing from you!

Contract Associate - Biotech

2009-12-16T19:30:22-05:00

CONTRACT ASSOCIATE - BIOTECH

Clinical Divide: When RFPs and Change orders come in, an objective eye is needed to scrutinize the bids and help to minimize out of scopes and change orders.

Project Scope: The Contact Associate will work with the Director of Clin Ops to evaluate and scrutinize RFPs for thoroughness and cost projections.
This role would also involve contract generation with CROs. This person will also look at actual spend vs forecast spending to adjust budgets as necessary.
This person would also attend bid defense meetings with CROs.

Project details. This is approximately 10 - 12 hours / month. Pharma/Biotech/Med Device experience only.
Work can be done offsite but will need to be onsite for CRO bid defense meetings

Compound Library Assistant

2009-12-16T17:35:31-05:00

Primary focus is the maintenance and organization of a massive compound library.

Operation of the automated robotic system for compound management, and also the semi-automated liquid handling workstations.

Experience with chemical databases is the key element for this role. The successful candidate will also have experience operating automation/robotic systems.

Additional experience working with HTS instrumention would be ideal.

Excellent verbal and written communication skills are a must.

The successful candidate will have a friendly, upbeat, team-oriented personality.

BS degree in a chemical and/or biological field with 2 years of industry experience in the above areas is desired.

CPhT with significant experience using automated pharma systems and databases may also be considered.

Research Associate - Immunoassay (Burlington, MA)

2009-12-16T15:56:40-05:00

Our client seeks an individual with experience with immunoassays and diagnostic devices. You will assist in the optimization of immunoassays and the transfer of these assays to manufacturing. We are looking for a detail-oriented individual who will operate in the fields of R&D, process optimization/validation and QC.

Responsibilities:

Design, perform and document experiments, typically quantitative analysis of proteins
Participate in the validation of manufacturing procedures by assessment of product performances.
Execute QC protocols for the manufacturing of microfluidic components. (Microscopic observations, Protein assays, Basic laboratory skills, Testing for product lot release to customers)
Assist in implementation of a quality system
Accomplish goals under tight time lines

Requirements:

BS/MS in Biology, Biochemistry, or related field with 3+ years of industry experience
Must have demonstrated ability to perform in a fast-paced entrepreneurial environment
Excellent attention to detail and ability to meet strict timelines
Clinical experience in a FDA regulated environment is a plus
Familiarity with clinical diagnostics and miniaturized devices is a plus

Please submit resume as word attachment to jobs@cwsciences.com

Must be US Citizen or Green Card Holder and Live Local

Commonweath Sciences, Inc.
http://www.cwsciences.com

Director, Medical Liaison Group

2009-12-16T11:05:26-05:00
Our client is in search of someone with a strong background as a medical science liaison, who is passionate about science and highly motivated, to join them as a Director of their Medical Liaison Group. This is a newly created group & function for our exciting client who�s about to file their first NDA! This person will assume overall responsibility for the medical liaison functions of the company as well as integrate Medical Affairs activities with other departments within the company. This person will manage the patient registry program as well as build and support an international community of physicians. This person is on the forefront, the face, of a truly life saving drug.

What is Required?
- A Ph.D. or PharmD in a Neuroscience related discipline
- 7+ years industry experience - need to have not only been an MSL but also have managed a team of MSL�s. This person will hire and manage a team of six people.
- Orphan drug experience - at least a little
- Outstanding communication skills and enjoyment of what comes along with being an MSL.

You will appreciate the ethics guiding each StratAcuity team member. We build lasting relationships with exceptional scientists and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a StratAcuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

StratAcuity Scientific, CHEMISTRY IS EVERYTHING.

ADME Profiling Scientist (Cambridge)

2009-12-16T10:54:34-05:00

ADME Profiling Scientist - Job #CL2146

DUTIES

This position focuses on in vitro permeability studies. The candidate will be responsible for developing, conducting and interpreting relevant artificial membrane, cell based, and drug transporter assays. Experience in validating and implementing automated assays would be a plus. The candidate will also be involved in the daily operation of the existing profiling assays with the agreed throughput, and interpretation of the data. The candidate must have the ability to work interactively on inter-disciplinary teams, have excellent communication skills to present at project team meetings, explain the data and offer scientific advice. It will be preferable that the candidate is able to draft scientific proposals and manuscripts/reports.

SKILLS

Good understanding of underlying principles of cell culturing, protein biochemistry is essential. Familiarity with PK/PD, bioanalysis, lab automation (robotics and plate readers) and knowledge in LCMS is a plus. Successful experience in working toward a timeline is favored. Excellent collaboration and communication skills, both written and oral, strong experimental and problem solving skills, as well as a track record of strong initiative and follow-through are required.

EDUCATION

BS +5 yrs, or M.S. +2 yrs in cell and molecular biology, drug metabolism/transporter, PK/PD, or related fields.

Candidates MUST live local and be a US Citizen or Permanent Resident Green Card Holder

Commonwealth Sciences Inc.
http://cwsciences.com

Please submit resumes to jobs@cwsciences.com and refer to job #CL2146

Marketing Coordinator (Cambridge)

2009-12-16T10:50:19-05:00
Marketing Coordinator - Job #CL2143

We are currently looking for a Marketing Coordinator that can join our team. This individual should have an understanding of science or marketing experience, have the ability to communicate clearly with people from diverse backgrounds, and enjoy a challenge. Fluency in Spanish and English required.

Duties:

Perform regional sales and market analysis within North, South and Central America and create marketing plans to increase sales in those segments.
Implement and/or develop working relationships with South and Central American Distributors. Set and meet sales targets for distributor countries.
Assist with the implementation and marketing of regional promotions.
Investigate and suggest new marketing (online and offline) opportunities.
Keep literature and promotional items organized in marketing closet and maintain an accurate inventory.
Coordinate and manage all aspects of company�s attendance at tradeshows and conferences.

Summary of Job Requirements:

BS in life science
1-3 years of experience within life science or marketing field.
Laboratory or industry experiences particularly within Biology/Biochemistry a plus.
Must have excellent oral and written communication skills in both English and Spanish. There will be a speaking and writing test to assess proficiency.
Must be able to travel 10-20% domestic and internationally.

Candidates MUST live local and be a US Citizen or Permanent Resident Green Card Holder

Please submit resumes to jobs@cwsciences.com and refer to job #CL2143

Commonwealth Sciences, Inc.
http://cwsciences.com

Histologist (Cambridge)

2009-12-16T10:17:31-05:00
DUTIES
In conformance with all SOPs and safety regulations, may perform (with minimal or no supervision) activities such as: necropsy, organ weighing, trimming, tissue processing, embedding, microtomy, cryotomy, routine & special staining techniques, immunohistochemistry, coverslipping, handling and weighing laboratory animals, QC, and archiving activities. May assist in maintaining inventory of necessary supplies. May obtain blood and bone marrow samples for clinical pathology testing and physiological specimens for either anatomic pathology or electron microscopy. May utilize slide scanning equipment and image analysis software. Will collect, verify and maintain study data, and measurements, and communicate results in an accurate and timely manner. May assist in the validation of new methodologies and instrumentation as needed. Will function on and/or lead teams assigned to major activities.

SKILLS
Strong personal and team-oriented time management skills.
Computer skills in Microsoft windows-based office software.
Demonstrated experience in the required area, and competency in all technical procedures.

EDUCATION
HT or HTL certification or equivalent, or AS/AAS degree with 4-6 years experience, or Bachelors + 5, or Masters + 3 years experience.

Candidates MUST live local and be a US Citizen or Permanent Resident Green Card Holder

Email resume to: jobs@cwsciences.com

Commonwealth Sciences, Inc.
http://www.cwsciences.com

S729, Accessioning Technician (Westborough, MA)

2009-12-16T09:54:32-05:00
SOFT's client, located in Westborough, MA needs an Accessioning for a contract position. Shift is Tuesday - Saturday, 8:30 A.M. - 5:00 P.M.

Duties: As an Accessioning Technician in the Westborough Accessioning Department the ideal candidate will:
- Unpack FedEx boxes and verify content
- Receive human specimens into the laboratory
- Verify requisition receipt and sample type
- Perform data entry into out computer system
- Enter test requisition information into computer system and label tubes
- Copy and collate paperwork and recognize inconsistencies in paperwork submitted
- Perform document imaging.
- Perform quality assurance check on paperwork and notify Client Services of incorrect or incomplete client practices (e.g. improper shipping containers, wrong/absent test requisition, etc.)
- Track receipt of local courier deliveries

All tasks must be performed using universal precautions against biohazard material.

Basic Qualifications: High school diploma and 0-2 years of experience using the Windows computer environment.

Preferred Qualifications: Previous data entry experience.

Please refer to the Position ID when inquiring about a job posting or sending in your resume.

***INDEPENDENT CONSULTANTS ONLY! NO THIRD PARTIES/NO SUB CONTRACTORS***

Jr. Validation Engineer (Northeast)

2009-12-16T09:52:43-05:00
Jr. Validation Engineer needed for a four month contract position located in the Northeast. Biotech experience is required. Assignment will include execution of IQ/OQ/PQ protocols; utilities and process equipment in a biotech facility. The time frame is mid to late February 2010. The project will pay an hourly rate + per diem if not local to the job site. Please submit resume for consideration.

Medical Information Associate-0901557 (Rockland, MA)

2009-12-15T18:32:24-05:00
At EMD Serono, Inc. our strength is our people!

About the Company

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.

Description
The Medical Information Associate is the primary contact in Medical Information to respond orally or in writing to medical and drug information questions regarding EMD Serono products to health care professionals and consumers. This includes responsibility for all processes related to receipt, response, resolution and documentation of these inquiries, within company standard operating procedures, regulatory requirements, and legal guidelines. The Medical Information Specialist is also responsible to document and triage reports of adverse events, product complaints, or other non-medical information inquiries or issues to the appropriate EMD Serono department.

KEY TASKS AND RESPONSIBILITIES:
Handles telephone and written communication from healthcare professionals, patients, and the general public.
Provides complete, timely and accurate oral and/or written responses to unsolicited requests for medical and drug information that can include information within or beyond product labeling and promotional materials(i.e., on- or off-label).
Prepares customized written responses that can incorporate standard response documents, literature searches, and/or articles in collaboration with Medical Information Specialists in accordance with department processes and company, industy, regulatory, and legal guidelines and requirements.
Assures payment of appropriate copyright fees to reduce legal risk to EMD Serono.
Monitors incoming inquiries to minimize regulatory and compliance risk to EMD Serono.
Obtains necessary documentation of unsolicitation of the request.
Monitors EMD Serono field-based personnel affiliation with submitted requests.
Documents in a timely manner in IRMS (Information Request Management System) all inquiries and responses and other actions associated with an external or internal customer within Medical Information.
Documents and validates in IRMS all medical, scientific, and other inquiries received by the after-hours medical information provider.
Receives, documents, and transfers adverse event or product complaint reports to US Product Surveillance and Quality Assurance.
Receives, documents, and triages inquiries unrelated to medical information to the appropriate EMD Serono department.
Provides basic information on EMD Serono clinical trials to prospective study subjects and investigators.
Prepares scheduled and develops ad hoc written reports from IRMS for trend analysis and tracking of inquiries received and responses delivered by Medical Information.
Liaises with Therapeutic Area Contact Center to align, where appropriate, work processes, call scripts, and training with those of Medical Information.
Creates and maintains verbal standard responses in collaboration with Medical Information Specialists.
Maintains knowledge that impacts the drug information and safety of all EMD Serono products, including literature, industry reports, and regulatory developments.
Alerts the appropriate therapeutic area business team of unusual trends or potential opportunities based on inquiries received.

Qualifications

EDUCATION & LANGUAGES
Healthcare degree (e.g., R.N, R.Ph., Pharm.D) preferred.
B.S. in an appropriate scientific major considered

PROFESSIONAL SKILLS & EXPERIENCE
1-3 years pharmaceutical-related industry experience in medical information and communications preferred.
Familiarity with medical terminology, medical literature, clinical research and documentation.
Other relevant experience considered (e.g., clinical pharmacy, clinical research, medical affairs, drug safety, hospital, drug information centers, call centers).

PERSONAL SKILLS & COMPETENCIES
Excellent oral and written communication skills to communicate professionally to healthcare professionals and patients.
Innovative approach to problem solving and solution orientation.
Proficiency in MS Office applications with knowledge of databases.
Experience with Lotus Notes and Information Request Management System (IRMS) is desirable.
Organizational skills and ability to follow projects to completion while adhering to company, regulatory, and legal guidelines and requirements.

Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0901557

Awards & Recognition

June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Associate I, Quality Control (Cambridge, MA)

2009-12-15T17:57:19-05:00
Temporary Assignment � 1yr assignment � hopes of turning perm.

Job Responsibilities:

1. Support biological activity assays for product release/stability testing of various
Biogen Idec pipeline programs.

2. Support routine laboratory systems and operations, including cell line maintenance.

3. Support qualification activities for data reduction software applications and sophisticated bioassay instrumentation.

4. Participate in method transfer/validation projects.

5. Author SOPs, qualification/validation protocols and reports
.
6. Contribute to continuous improvement initiatives.

Qualifications:
1. 1-3 years of relevant experience in a bioanalytical laboratory/environment (preferably cGMP regulated). Assay experience should include ELISA and/or other cell-based assays.

2. Aseptic technique and cell culture experience required.

3. Hands-on experience with software and/or instrumentation qualifications desired.

4. Demonstrated laboratory, computer, documentation/writing and organizational skills, as well as excellent communication skills.

BS in Biology, Biochemistry, Microbiology or other related field of study.

Biosciences technical writer (metrowest)

2009-12-15T16:12:22-05:00
Contract opportunity for EXPERIENCED biosciences writer (specifically, bioprocess filtration products) writing numerous instruction sheets and user manuals for a product launch. Documents must be written according to corporate style guidelines. Must be available for in-person meetings in metrowest area. Please provide your resume and link or website with writing samples. Please do not apply if you are not experienced, there will not be a lot of "ramp up" time available...candidate will be expected to understand products.

RESEARCH TECHNICIAN - Biomedical Engineering (Medford)

2009-12-15T14:32:58-05:00

This position is a 2-year limited appointment with the possibility of an extension based on continued grant funding. As this position is grant-funded it is not eligible for severance pay.

The Biomedical Engineering Department is a multi-disciplinary department that offers comprehensive research opportunities for those interested in the field, with significant emphasis on areas such as biomaterials, drug delivery, and tissue engineering. A research initiative on the development of platform technologies for the controlled, sustained release of pharmaceuticals has been funded in the Department of Biomedical Engineering at Tufts. This particular initiative focuses on biomaterials preparation, characterization and optimization for biocompatibility in vitro and in vivo for a sustained drug delivery system.

The key responsibilities for the Research Technician include but are not limited to: collecting, organizing, analyzing, and reporting scientific data. The Research Technician will be responsible for carrying out laboratory experiments. She/he will also be primarily responsible for carrying out high throughput material-drug screening experiments, biomaterial preparation and characterization, as well as drug loading and release studies. The Research Technician must be self-motivated and have superb communication/organizational skills. He/she must also be able to collect, organize, and report scientific data with proficiency.

Basic Requirements:

Bachelor of Science in a scientific or engineering discipline

0-2 years of lab experience

Experience in standard biochemistry/molecular biology techniques, proficient in Microsoft Office

Preferred Qualifications:The ideal candidate will possess 2+ years of lab experience (industry preferred). Previous experience with drug formulation/delivery is desirable, as is any previous experience with liquid handling robotic devices and the use and maintenance of one or more analytical methods (e.g., HPLC, MS) and or biochemical assays (ELISA, SDS-PAGE, etc.). Previous experience in a pharmaceutical research lab is also a plus.

Tufts University is an AA/EOE employer and actively seeks candidates from diverse backgrounds.
Apply Here

Technician (Brigham and Women's Hospital)

2009-12-15T14:32:44-05:00
Position available for a Research Technician in a basic science lab at the Channing Laboratory of Brigham and Women�s Hospital and Harvard Medical School. We study immune responses to corneal and lung infections caused by bacteria such as Pseudomonas aeruginosa. We use a variety of approaches including mouse models of infection, microbiology, immunology, cell biology, and molecular biology.

This position involves conducting experiments as well as laboratory maintenance responsibilities. A bachelor's degree (BA/BS) in biological sciences and some laboratory experience (e.g. lab classes) are required. One year of lab experience will be highly beneficial. This position will require work with animals, including surgical procedures. A commitment of at least 2 years is required. This is an excellent opportunity for someone interested in exploring a career in science or medicine or for an experienced technician interested in a disease-related project. Candidates who can start as soon as possible are desired.

Please respond by email with:
1. cover letter briefly explaining your career goals
2. resume including contact information for 2-3 people who will serve as references

Software Trainer and Junior Rails Developer (Boston, MA)

2009-12-15T14:25:11-05:00
Software Trainer and Junior Rails Developer (Part-time to full-time role)

Description:
Are you experienced in working with Ruby on Rails? Are you passionate about your craft and excited learning new web technologies that provide real solutions? Are you comfortable speaking to people in group settings? If so, you may be interested in joining our team!

We are a small-team looking for a part-time person to join our team. This person would start in a part-time role training users on our web application. We would like this person to join our product development team with a vision of transitioning to being a full-time developer/trainer in early 2010.

Implementation responsibilities:
* Conduct quality training courses to academic life science researchers (in person and web-based) on features and operations of the iLab software suite
* Use the iLab web application to set up new users and groups
* Handle scheduling of training rooms
* Achieve our researcher satisfaction goals
* Perform testing functions of the web application relevant to training
* Travel to local-area Boston hospitals (located in Longwood Medical Area, Kendall Square, Charlestown, etc).

Product development responsibilities:
* Web application development
* Usability engineering
* User interface development
* Requirements gathering

Qualifications (Required):
* Good attitude, works well with people
* Strong verbal and written communication skills
* Comfortable speaking to large groups of people
* Basic familiarity with web-based applications
* Experience with Ruby on Rails or similar web application framework

Additional Qualifications (Desired):
* 1-3 years experience in life sciences environment preferred
* 1-3 years experience in ruby on rails development preferred
* Proficiency in Microsoft Word, Excel, PowerPoint preferred
* Experience delivering software training using web and telephone conferencing tools
* Familiarity with CSS, AJAX, JavaScript technologies
* Experience developing and deploying complex web applications

Pay: $12 to $18/hour (dependent on experience). Transition to salaried role dependent on success.

Job Location: Boston, MA

Company URL:
http://www.ilabsolutions.com/

Company Profile:
Founded in 2006, iLab Solutions provides scientific organizations with unique tools to integrate materials management into the scientific process. iLab's research management and product selection tools enable researchers to share knowledge, track resources, manage budgets, and make smarter purchasing decisions. Whether integrated with existing procurement systems or with iLab�s own hosted catalogs and approval management tools, the intuitive user interface drives adoption and 90%+ end user satisfaction.

The iLab system was developed in partnership with scientists at leading NIH-funded research hospitals and universities. Researchers at top academic research organizations and biotechnology companies use the iLab system on a daily basis. Through an ongoing dialogue with researchers and administrators, the iLab team continually enhances system functionality and the user experience.

Bioinformatics Engineer II (Boston, MA)

2009-12-15T14:06:27-05:00
Job description:

General Summary: Design and implement next generation, multi-tier Java/J2EE software applications to support genomic research. Familiarity with a wide range of existing databases and tools, and familiarity with principles of experimental design and modern data analysis paradigms are required, and excellent interpersonal skills.

Primary Duties and Responsibilities:
-- Design, develop, and implement multi-tier software applications to support genomic research
-- Work with project managers and the development team to design use cases, write functional specifications, and development timelines and milestones
-- Evaluate existing and emerging technologies to help select the most suitable tools for the tasks at hand
-- As a member of the development team, work to establish best practices for all phases of the application development lifecycle, including design, development, testing, release, and maintenance
-- Write technical documentation and tutorials

Requirements:

Bachelors degree required, MS preferred or PhD in bioinformatics, computer science and/or the life sciences and 3-5 years relevant experience. Performs primary duties as above and has progressed to performing more advanced skillsets as directed. Requires general supervision with latitude for independent judgment.

Knowledge, skills and abilities required:
-- Extensive experience with Java technologies/frameworks for multi-tier application development such as Spring, Hibernate, J2EE, Struts
-- Familiarity with a wide range of biological databases and resources, including, but not limited to GenBank, EnsEMBL, the UCSC genome browser, Reactome, and other similar resources
-- Familiarity with genomic technologies and their applications, including experimental design considerations
-- Authentication frameworks/application security
-- Experience with data-intensive hosted applications
-- Expertise with database design and implementation desirable
-- Skilled in both Windows/Unix environments
-- SVN and best practices around source code control
-- Ability to work in fast paced, agile development environment
-- Knowledge of standard concepts, practices, and procedures of software development
-- Excellent problem-solving, organizational, and people skills
-- Experience with high-performance computing desirable

To apply, please visit our website: http://www.danafarbercareers.com Job ID 19131

EHS Safety Officer (Cambridge Area)

2009-12-15T12:29:12-05:00
Safety Partners, Inc.
Open Positions

JOB TITLE: Consulting Safety Officer (CSO)

DEPARTMENT: Environmental and Occupational Health & Safety (EHS) Program Development and Consulting

Reports to: Supervisor Consulting Safety Officer
Annual review by the Supervisor

Level: CSO
Work Hours: Full Time
Employment Status: Non-exempt

MAIN PURPOSE OF JOB
Our CSO��s provide environmental health & safety (EHS) program development and support consultation services to Safety Partners�� clients. Coordinate clients�� EHS program development and implementation for general safety, chemical safety, biosafety and radiation safety, and/or perform specific EHS tasks as designated by the client boss.

MAIN JOB DUTIES/RESPONSIBILITIES
* On-site client work, with the goal of supporting clients�� EHS programs for workplace safety and for local, state and federal regulatory compliance. EHS program development and implementation for general safety, chemical safety, biosafety and radiation safety. Working with clients to implement policies and procedures for procurement, use and disposal of hazardous materials, including, but not limited to:

* Manage, develop, implement radiation safety, biosafety, chemical safety programs - procurement, use, disposal
* Manage, develop, and implement General Safety Program - basic life safety: general fire safety, hazard awareness, emergency preparedness.
* Develop and maintain all OSHA specific safety programs.
* Carry over relevant elements of safety program throughout client site, including: animal facility, machine shop, engineering, warehouse, shipping & receiving, office/admin.
* Coordinate and facilitate safety committee.
* EHS permitting for procurement / storage / use / disposal of hazardous materials: flammables, rDNA, select agents, MWRA, controlled substances, DEP, EPA, radiation, etc. Environmental permitting may be done upon approval of the Director and President.
* Coordinate hazardous waste segregation, collection, disposal. This may include waste pouring.
* Review hazardous materials ordering, usage & storage to maintain compliance and safety.
* Audit operations to confirm that EHS program components are being observed.
* Training client staff to ensure regulatory compliance and to ensure staff and Safety Officers are integrated into the safety program.
* Maintain central safety files.
* Develop & deliver training for all safety programs relevant to client, including, but not limited to Emergency Preparedness, HazCom, Lab Stand, Chem Awareness, Biosafety, Bloodborne Pathogens, Radiation Safety
* Coordinate specialized training, such as RCRA, DOT, IATA, OSHA First Responder, Wastewater Operator, CPR, First Aid, AED.

If you feel you are qualified for this position, please e-mail a copy of your resume to: jbergeron@safetypartnersinc.com or fax to : 928-447-1040.

For more information about Safety Partners, Inc, please visit: http://www.safetypartnersinc.com

Project Engineer (Burlington, MA)

2009-12-15T11:23:35-05:00
Project Engineer� Job # 28048

Position Description
Working under the general direction of a senior engineer or project manager, complete assigned environmental health and safety projects. May work independently on smaller projects. Responsible for implementation of defined scope within schedule and budget. Responsible for technical accuracy and practicality of solutions.

Candidates should have 0-7 years of experience.

Education Requirements
BS Engineering (prefer environmental, civil, mechanical or chemical)

Specify Registration Requirements
EIT is a plus with interest in obtaining PE

Company Overview
EBI Consulting is a rapidly growing, profitable company, headquartered in Burlington, MA. Our employees are the key to maintaining our competitive edge. To attract and retain the best industry talent EBI shares its success with its employees, and is committed to providing a professional work environment where career learning, growth and recognition are highly valued. If you are seeking an opportunity to work in a progressive organization that will offer you diversified challenges and an excellent opportunity for advancement please review our current employment opportunities. For more information about EBI and open positions please visit our website at www.ebiconsulting.com.

Benefits
EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities.
EOE M/W/D/V

Submittal
Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com. You must include the following information:

1. Reference job #, job title and resource
2. Brief summary of past related experience (highlight your experience as it relates to our need & industry);
3. List of your education credentials and professional registrations
4. Salary history

We look forward to hearing from you!

Research Technician (Boston)

2009-12-15T11:16:47-05:00
Leading academic research institution in the Longwood Medical Area of Boston has an opening for a Research Technician.

PREVIOUS EXPERIENCE IN CELL CULTURE WORK IS A MUST.
---------------------------------------------------------------------------------------------------------

The research technician will conduct experiments aimed at optimizing culture conditions for protein expression in Sf9 cells, assist in protein purification and contribute to the development of new methodologies. This will require the candidate to be capable of analyzing assays, Western blots, and cell growth and survival patterns.
The candidate will also be expected to remain current on the relevant literature and provide documentation of work progress at the weekly laboratory meetings.

Please reply to this posting with a CV and cover letter (in WORD, Plain text or PDF format). Please highlight relevant cell culture experience and your current visa status (if applicable).

Histologist Opportunity (Cambridge, MA)

2009-12-15T10:12:07-05:00
We have a Contract opportunity with a prominent client for a Histologist in Cambridge, MA.

DUTIES >>
May perform (with minimal or no supervision) activities such as: necropsy, organ weighing, trimming, tissue processing, embedding, microtomy, cryotomy, routine & special staining techniques, immunohistochemistry, cover slipping, handling and weighing laboratory animals, QC, and archiving activities.
May assist in maintaining inventory of necessary supplies.
May obtain blood and bone marrow samples for clinical pathology testing and physiological specimens for either anatomic pathology or electron microscopy.
May utilize slide scanning equipment and image analysis software.
Will collect, verify and maintain study data, and measurements, and communicate results in an accurate and timely manner.
May assist in the validation of new methodologies and instrumentation as needed.
Will function on and/or lead teams assigned to major activities.

SKILLS >>

� Strong personal and team-oriented time management skills.

� Computer skills in Microsoft windows-based office software.

� Demonstrated experience in the required area, and competency in all technical

procedures.

EDUCATION >>

� HT or HTL certification or equivalent, or AS/AAS degree with 4-6 years experience, or

Bachelor�s + 5, or Masters + 3 years experience.

For immediate consideration, please forward a current copy of your Word formatted resume

Manager, Cancer Genome Projects (Cambridge, MA)

2009-12-15T09:13:53-05:00

OVERALL RESPONSIBILITIES

Manages a portfolio of projects with a focus on using next generation sequencing in medical genetics research. Serves a point of contact between Broad project teams and project investigators for all stages of project initiation, project tracking and delivery of data. Coordinates with multiple Broad Institute Platforms to ensure appropriate sample hand off, project tracking and delivery of data in a timely and efficient fashion to meet the scientific objectives. Manages communication with Program leadership and scientists to ensure project goals and expectations are clear and that teams provide timely feedback on project progress or blocking issues.

CHARACTERISTIC DUTIES

- Serves as the primary contact point between program investigators and platform staff to ensure work proceeds in a coordinated, efficient manner.

- The projects to be managed will involve utilization of multiple technology platforms, including large scale re-sequencing and SNP genotyping by large-scale, array-based methods.

- Manages all aspects of the projects, from initial project consultation, coordination of receiving samples and QC, scheduling of work with platform managers, data review and data delivery.

- Gathers information on IRB approvals and ensures appropriate sign off for sample sets given status of informed consent and data release requirements.

- In collaboration with Technology Platform managers, troubleshoots and monitors quality of projects throughout production process.

- Ensures that projects meet critical milestones and that work remains within budget.

- Works to anticipate needs of program investigators and platform team, including reporting on project status and delivery of results.

- Presents project summaries to internal and external project teams.

- Other related tasks as required.

SUPERVISION EXERCISED

No formal supervisor responsibility. May need to guide others, and will need to build support among diverse groups.

QUALIFICATIONS

- Ph.D. (preferred) in biology or related field or equivalent combination of education and experience.
- Directly related industry experience preferred.
- At least 5 years proven Project Management experience required.
- Should have direct experience or should be highly familiar with genomic methodologies such as sequencing and array-based genotyping including technical aspects, quality control, and current methods of data analysis. Must possess the management and communication skills suited to a professional research organization. Ability to work in a highly collaborative environment and excellent communication and presentation skills essential.

The Broad Institute was launched to pioneer a new model of collaborative biomedical science that would transform medicine. To accomplish these goals, we have built an amazing team of talented “Broadies” who work together to realize this transformation.

We are always looking for new Broadies to join our team and help us tackle important problems at the cutting edge of science.

The Broad community

The Broad community includes professional scientists from many disciplines, administrative staff, and students. We seek to cultivate an interdisciplinary, goal-oriented work environment that unleashes scientific creativity and empowers our people to pursue ambitious and critical projects.
Our work transcends traditional academic boundaries, giving Broad employees and affiliates access to an unparalleled biomedical research community across the Harvard and MIT communities and beyond.

Benefits of working at Broad

The Broad Institute is committed to providing its employees with a competitive compensation and benefits package. We recognize the need for our employees to have a balance between work and personal life. To that end, our benefit plans and options reflect our desire to promote an environment that supports the health, diversity, and general wellbeing of our employees.

All Broadies also have access to world-class research and state of the art technology and are fully supported in their professional development, pushing the envelope for further growth.

The Broad Benefits Program includes:

- Medical: choice from 2 HMOs and 1 PPO. Broad pays 80% of premiums.
- Dental: 1 enriched plan. Broad pays 80% of the premiums.
- Basic Life Insurance, Accidental Death & Dismemberment, Business Travel paid in full by Broad
- Supplemental Life Insurance choices for yourself, your spouse and children
- Short-Term and Long-Term Disability paid in full by Broad
- Flexible Spending Accounts, Health care, Dependent care, and Parking
- 401(K) Plan w/ 6% Employer Match, and Annual Contribution (discretionary but targeted at 4% for 2010)
- 4 Weeks of Vacation after 1 Year
- Tuition Reimbursement - 1 class each semester at MIT/Harvard paid in full (2 per year maximum)
- Identity Theft Prevention and Insurance paid in full by Broad
- Estate Planning - free will preparation
- Adoption Assistance
- Employee Assistance Program (EAP)
- MBTA Commuter & Transportation Subsidies (50% up to the federal maximum)
- Subsidized onsite parking, occasional parking, van pool, and car pool programs available
- Parents in a Pinch Back Up Child Care
- Credit Union
- Discounted Fitness and Gym memberships
- Pet Insurance
- Group Home & Auto Insurance
- Group Legal Program

The Broad Institute is an equal opportunity employer.

If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id=846774-1857-9139

Research Assistant (Cambridge)

2009-12-14T15:42:21-05:00
Scientists at Cellay, Inc. have developed novel nucleic acid probes and labeling methods that offer several advantages
for the emerging field of molecular diagnostics. Probes are highly specific, hybridize rapidly, generate robust signals,
and can be used in multi-color panels.

In addition, since the company is launching products for preimplantation genetic diagnostics, cancer diagnostics,
you will participate in several commercial aspects of product development.

If your career plans will require use of fluorescence in situ hybridization (FISH), exposure to genetics, and you thrive
in a small company atmosphere in which you can take charge, this position is an excellent opportunity to work with experts.

Qualifications: BA and related job experience.

Location:

We are located in Inman Square in Cambridge, close to bus stops and the Central Square T-stop.

Compensation is commensurate with experience.

No phone calls; no recruiters.

Please e-mail cover letter and resume with salary requirements

Technical Assistant I - Lodish Lab (Cambridge, MA)

2009-12-14T15:23:06-05:00
OVERALL RESPONSIBILITY

Designs and performs bench level experiments and small independent research projects to support scientific research aimed at identifying genes that regulate metalloprotease cleavage of substrates like EGF ligands, with the goal of developing new therapies for cancer, heart disease and kidney disease. Analyzes experimental data, addresses methodological problems in experimental protocols and results, and reports data to supervisor. Uses discretion in prioritizing and organizing workflow and in optimizing methodologies and results.

CHARACTERISTIC DUTIES

� Major Responsibilities include: standard molecular biology assays, cell culture, flow cytometry
� In consultation with the Principal Investigator or other project manager, designs and conducts bench level experiments and small independent research projects.
� Independently operates lab equipment and prepares, orders, and maintains stocks of necessary reagents, solutions and supplies. May work with vendors to address equipment, reagent, or supply issues.
� Performs analysis of experimental results by identifying methodological problems and helping to identify and implement modifications in research protocols.
� Documents, compiles and assists in interpreting experimental data. Reports data to supervisor in oral and written reports.
� May assist Technical Associate or project manager with determining the order of research processes that best support essential project goals.
� Operate and maintain laboratory equipment to complete investigations.
� May consult scientific literature as needed.
� Other tasks as required or assigned.

QUALIFICATIONS

� Bachelor�s degree in Biology or related field
� 1 year of experience working in a research laboratory preferred.
� Proficiency in basic lab techniques and principles of molecular biology required.
� Knowledge of various scientific databases required.
� Excellent written and oral communication skills, strong organizational skills required.

Interested candidates should send resume to:
Rodney Byrd
The Whitehead Institute for Biomedical Research
9 Cambridge Center
Cambridge, MA 02142
resumes@wi.mit.edu

Clinical Research Associate (Andover, MA)

2009-12-14T15:21:54-05:00
Position Summary:
This position will contribute, under general direction, to the coordination and performance of activities related to pre- and post-market clinical research in the US in accordance with FDA regulations. Collaboration with US and International counterparts during the development of clinical research projects will be required. Alignment with marketing objectives to ensure endpoints meet the desired claims will require collaborative relationships with Marketing as well as other functions as required.

Major Responsibilities of the Position:
-Develop clinical study documentation including clinical research protocols, informed consent documents, and Case Report Forms
-Conduct monitoring visits (e.g., initiation, routine, and close-out) to ensure adequate enrollment, follow-up, training, product availability, etc., according to the study protocol and FDA regulations
-Prepare monitoring visit reports
-Management of key aspects of post-market clinical studies, which may include:
--Study design, budgets, and planning
--IRB submissions
--Site recruitment
--Site agreement/budget negotiations
--Site management
--Essential document collection
--Product inventory and device accountability
--Project tracking document maintenance
--Data management
--Adverse event reporting
--Investigator meetings
--CRO management
--Study trial master file maintenance
--Compliance with regulatory guidelines

Other Duties:
-Assist investigators with presentations, etc., as needed
-Assist in the development and/or maintenance of the clinical department infrastructure such as drafting or reviewing SOPs and Work Instructions
-Liaise with customers who are interested in Investigator Initiated Research
-Other tasks as assigned

Minimum Qualifications:
-Minimum 2-5 years Clinical Research experience with on-site monitoring experience
-Knowledge of clinical study management
-Demonstrated knowledge and adherence to FDA regulations and GCP
-Excellent interpersonal, organizational, and communication skills
-Ability to work well on multiple tasks in a team environment as well as be a self-starter/initiator
-Ability to travel up to 50%
-Proficiency in Microsoft Applications (Word, Excel, PowerPoint, Access)
-SAP experience desirable

Required Knowledge and Skills:
-Bachelors degree (preferably in science/health field or biomedical engineering)
-External clinical research training desired

Work Environment and Physical Demands:
General office environment. No special physical demands required.

HOW TO APPLY:
Please apply directly through our website: http://www.straumann.us and click the "Jobs" link at the top of the page.
Be sure to upload the following documents for consideration:
1. Cover Letter
2. Resume
3. Writing Sample

Absolutely no recruiters on this position. Thank you for your consideration and respect.

Lead Generation / Sales Support (Hyde Park)

2009-12-14T14:05:25-05:00
About Us:
Overbrook Scientific is looking for competitive, results oriented Lead Generation and Sales Support staff to work in a high energy, fast-paced entrepreneurial environment. Overbrook Scientific purchases and sells state of the art Analytical and Life Science instrumentation and services to laboratories worldwide. Our company works directly with a wide variety of market segments including Biotechnology, Pharmaceutical, Environmental Testing, Materials Science and Food and Beverage.

The candidate must be able to:
Generate a large volume of outgoing telephone calls per day.
Interact easily with independent business owners, laboratory directors, managers and purchasing agents.
Identify, qualify and engage decision makers quickly.
Be detail conscious and grasp quickly, multiple product lines and their respective science.
Offer inside sales support including quote generation and client follow up.

The candidate must also possess an entrepreneurial spirit with an ability to produce leads (laboratory or science background a plus), and have an upbeat and enthusiastic attitude with excellent verbal skills.

The position can be full or part time (minimum 24 hrs/week) and can be an entry level position to full time sales over time.

For immediate consideration, please submit a resume and cover letter.

PhD editors for scientific video journal (Cambridge/Somerville - Davis Square)

2009-12-14T10:53:51-05:00
JoVE is a young scientific publishing company developing a new type of scientific journal using video online. We are looking for energetic individuals to grow the journal content in specific areas of life sciences (Medicine, Neuroscience, Immunology, Bioengineering and Plant Biology). The responsibilities will include developing and recruiting the content from academic labs.

Requirements:
- Ph.D. or MD degree with a good knowledge in one of the areas: Neuroscience, Immunology, Bioengineering or Plant Biology
- experience in marketing or sales or fundraising. Must be able to effectively communicate with people, by phone and email.
- be organized, energetic and independent

We are looking for people who will start working part-time and become full-time if successful.

JoVE is a young dynamic start-up. Our office is very close to the Davis Square Red Line T station.

Please send your resume and a short description of your relevant experience.

Research Assistant Acupuncture Study (Newton, MA)

2009-12-13T18:55:25-05:00
Research Assistant
Hours-10-20

General description:
This position will be to assist in the ongoing clinical study of the treatment of Gulf War Illness with acupuncture. The study is 100% funded by a grant from the US Department of Defense. This individual will interact with a team of senior and junior investigators, students, fellows, and other clinical research staff members.

Duties include:
� assisting with recruitment, screening and interviewing adult participants in ongoing clinical studies
� help to recruit and screen potential study participants according to protocol's inclusion and exclusion criteria
� ensure the applicant be knowledgeable of the protocol so that study activities are completed smoothly, correctly, and completely
� conduct baseline and follow-up interviews over the phone or in person
� administer questionnaires, complete basic research screening and complete procedures (such as blood draw) as required by the study protocol.
� processing and organization of human blood and serum samples
� assist in data base development, data input and organization of study related materials
� frequent travel to obtain consent and collect blood samples and screening data
� other duties as assigned

Qualifications:

Must possess excellent interpersonal skills and be able to work with adults.

High school diploma/GED required. Bachelor�s degree preferred. Two years related experience required. Additional education may substitute for experience. Ability to draw blood is required. Phlebotomy certification preferred.

Position Hours: Monday-Friday and some Saturdays
Salary Range: $11.84 - $16.27
Contact: Lisa Conboy, New England School of Acupuncture, lconboy@nesa.edu

Research Associate

2009-12-13T18:44:59-05:00
Projects: Studies of Stress, Health, and Healthcare Use Among Military and Veteran Populations

Job Description: Seeking a full-time Research Associate to work on a research team involved with several projects in related areas. The primary projects are as follows: (1) updating and evaluating an educational intervention to foster enhanced sensitivity toward and knowledge of women veterans among Veterans Administration (VA) staff; (2) updating widely used scales for assessing deployment stressors implicated in the post-deployment mental health and adjustment of military and veteran populations; and (3) examining gender, stigma, and other barriers to health care for veterans. In addition, this individual will have the opportunity to get involved in other research projects in related areas, and will have access to existing datasets for the purpose of manuscript preparation and conference presentations. The Research Associate will work as part of a small research team, and will take the lead in several of the day-to-day aspects of these projects. With supervision from the Principal Investigator this individual will be responsible for managing all aspects of data administration, and will also be heavily involved with data analysis and the preparation of research findings in the form of manuscripts and conference presentations. This individual will also assist in the training and guidance of junior research assistants, and contribute to grant application preparation. Annual salary for a full-time PhD-level candidate will be approximately $61,425; annual salary for a full-time Masters-level candidate will be approximately $50,769.

Requirements: Masters or Doctoral degree in experimental psychology (preferably, with a background in social or health psychology), clinical psychology, or public health; proficient at managing all aspects of data administration and management; strong organizational and interpersonal skills. Interest in women�s health preferred.

Time Commitment: Two years, with possibility of an extension.

Anticipated Start Date: April � June, 2010

Contact: Brian Smith, Ph.D., Brian.Smith12@va.gov, 857-364-6196; Women�s Health Sciences Division, National Center for Posttraumatic Stress Disorder (116B-3), VA Boston Healthcare System, 150 South Huntington Avenue, Boston, MA 02130.

The Department of Veteran Affairs is an Equal Opportunity Employer.

Psychology Research Assistant

2009-12-13T18:37:54-05:00
Projects: Studies of Stress, Health, and Healthcare Use Among Military and Veteran Populations

Job Description: Seeking a full-time Research Assistant to work on a research team involved with several projects in related areas. The primary projects are as follows: (1) updating and evaluating an educational intervention to foster enhanced sensitivity toward and knowledge of women veterans among Veterans Administration (VA) staff; (2) updating widely used scales for assessing deployment stressors implicated in the post-deployment mental health and adjustment of military and veteran populations; and (3) examining gender, stigma, and other barriers to health care for veterans. With supervision from the Principal Investigator and Project Coordinator, this individual will be involved in many tasks associated with study preparation, implementation, and dissemination. Duties will include, but not be limited to, the following: conducting and maintaining background literature searches, organizing study files and data, assisting in the preparation of research findings in the form of manuscripts and conference presentations, and assisting in the preparation of grant applications and IRB submissions. Annual salary for a full-time bachelors-level candidate will be approximately $41,505.

Requirements: Bachelors degree in psychology or a closely related discipline; research experience.

Time Commitment: Two years, with the possibility of an extension.

Anticipated Start Date: April � June, 2010

Applicants should send or arrange for: 1) a letter describing their interest in the position and related career goals, 2) a curriculum vita or resume, 3) a current transcript, and 4) at least one letter of recommendation to:

Brian N. Smith, PhD
Women�s Health Sciences Division
National Center for PTSD (116B-3)
VA Boston Healthcare System
150 South Huntington Ave.
Boston, MA 02130-4817
Ph: 857-364-6196

For electronic submissions or further information: Brian.Smith12@va.gov

The Department of Veteran Affairs is an Equal Opportunity Employer.

Technical Assistant position is immediately available at a cancer biol (Harvard Medical School, Brigham & Women�)

2009-12-13T13:48:23-05:00
Position Available: Technical Assistant position is immediately available at a cancer biology /stem cell laboratory.

Employer: Harvard Medical School, Brigham & Women�s Hospital, Department of Pathology to work in the lab of Dr. Tan Ince, MD, PhD.

Research Focus: Tumor stem cell biology.

Disease Area: Breast and ovarian cancer.

Contact: Applicants should submit (by email to tihmsbwh@gmail.com) their curriculum vitae, list of publications and experience, contact information for three references, a description of their current research, and a brief vision for future objectives and career plans.

Research Projects:
a) Tumor Stem Cell Epigenome: This is a highly collaborative project that is designed to identify breast tumor stem cell-specific histone modification and DNA-methylation patterns and map transcription factor networks that regulate tumor stem cell phenotype.
b) Heat Shock Proteins (HSP): This project is designed to examine regulation of tumor stem cell biology by Heat Shock Proteins (HSP) and its influence on breast cancer phenotype in collaboration with a renowned HSP lab.
c) Development of Culture Media: Our laboratory has specific expertise in developing chemically defined cell culture media specially designed to grow normal and malignant human epithelial and stem cells.
d) Systematic Genotype/Phenotype Correlations: This project is designed to map the oncogenic pathways that cause malignant behavior in genetically engineered malignant mesothelioma cells.
e) Analysis of Cell-of-origin/Oncogene Cooperation: This project is designed to determine the cell origin of different human breast and ovarian carcinomas.

Laboratory environment: The laboratory is located in a highly interactive and highly dynamic department and we collaborate extensively with many renowned experts within and outside Harvard community on specific projects. Our laboratory has extensive expertise in human and mouse Pathology and Pharmacology and has either developed or adapted many of the methods routinely used in the lab including; 1) Highly sophisticated cell-type-specific 2D/3D in vitro tissue culture models, 2) in vivo tumor xenograft models 3) cell type specific chemically-defined media systems, 4) genetically engineered human breast and ovarian cancer cells, and malignant mesotheliomas, 5) analysis of normal and tumor human tissues at the DNA, RNA and protein level. The principal investigator has twenty years of post-graduate basic and translational research experience with expertise in cell and molecular biology, medicine, pathology and pharmacology.

Requirements:
Training Required: Minimum 1-2 years of bench work experience is required.
Location and time commitment: Minimum 2 years commitment and ability to re-locate within the US (anticipated summer 2010).
Required Skills: Job Skills: Competence in basic mammalian cell culture and molecular biology methods such as western blots is absolutely required. Other skills in DNA subcloning, PCR, Southern blots and Northern blots and FACS isolation of cells, facility with handling mice such as intravenous and orthotopic injections, and necropsy of tumor bearing mice is preferred. Candidates should have a good command of the English language and should be available for an interview.
Relevant References and Publications:
1. Ince TA, et al. Transformation of distinct human breast epithelial cell types leads to different tumor phenotypes. Cancer Cell 2007;12 (2):160-170. 15.
2. Park IH, Zhao R, West JA, Yabuuchi A, Huo H, Ince TA, Lerou PH, Lensch MW, and Daley GQ. Reprogramming of human somatic cells to pluripotency with defined factors. 451:141-6, Nature, 2008.
3. Lerou PH, Yabuuchi A, Huo H, Takeuchi A, Shea J, Cimini T, Ince TA, Ginsburg SE, Racowsky C, and Daley GQ. Human Embryonic Stem Cell Derivation from Poor-Quality Embryos. 26:212-4, Nat Biotechnol. 2008.
4. McAllister SS, Gifford AM, Greiner AL, Kelleher SP, Saelzler MP, Ince TA, Reinhardt F, Harris LN, Hylander BL, Repasky EA, Weinberg RA. Systemic endocrine instigation of indolent tumor growth requires osteopontin. 13;133(6):994-1005, Cell, 2008.
5. Godar S, Ince TA, Bell GW, Feldser D, Donaher JL, Bergh J, Liu A, Miu K, Watnick RS, Reinhardt F, McAllister SS, Jacks T, Weinberg RA. Growth-Inhibitory and Tumor- Suppressive Functions of p53 Depend on Its Repression of CD44 Expression. 11;134(1):62-73. Cell, 2008.
6. Lin MC, Lomo L, Baak JP, Eng C, Ince TA, Crum CP, Mutter GL. Squamous morules are functionally inert elements of premalignant endometrial neoplasia. 22(2):167-74, Mod Pathol, 2009.
7. Elmasri H, Karaaslan C, Teper Y, Ghelfi E, Weng M, Ince TA, Kozakewich H, Bischoff J, Cataltepe S. Fatty acid binding protein 4 is a target of VEGF and a regulator of cell proliferation in endothelial cells. FASEB J. 2009.
8. Chan EM, Ratanasirintrawoot S, Park IH, Manos PD, Loh YH, Huo H, Miller JD, Hartung O, Rho J, Ince TA, Daley GQ, Schlaeger TM. Live cell imaging distinguishes bona fide human iPS cells from partially reprogrammed cells. Nat Biotechnol. 2009 Oct 11.
9. Dinulescu D, Ince TA, Quade BJ, Crowley D and Jacks T. Role of Oncogenic K-RAS in the Development of Endometriosis and Endometrioid Ovarian Adenocarcinoma. Nat Med. 2005;11(1):63-70
10. Team finds way to create cancer stem cells. http://web.mit.edu/newsoffice/2007/breast-cancer-0813.html
11. Research Highlights. On the origins of tumor subtypes. Nature Cancer Reviews, Sept. 2007 http://www.nature.com/nrc/journal/v7/n10/full/nrc2234.html
12. http://www.wi.mit.edu/news/archives/2007/rw_0813.html
13. http://www.bcrfcure.org/action_0708grantees_ince.html
14. http://www.marf.org/Resources/Research/2005Research.html

Post-doctoral Position is immediately available at a cancer biology /s (Harvard Medical School, Brigham and Wome)

2009-12-13T13:45:47-05:00
Position Available: Post-doctoral Position is immediately available at a cancer biology /stem cell laboratory.

Employer: Harvard Medical School, Brigham and Women�s Hospital, Department of Pathology to work in the laboratory of Dr. Tan Ince, MD, PhD.

Research Focus: Tumor stem cell biology.
http://www.dfhcc.harvard.edu/membership/profile/member/1193/0/
http://www.bcrfcure.org/action_0809grantees_ince.html

Disease Area: Breast cancer and ovarian cancer.

Contact: Applicants should submit (by email to tihmsbwh@gmail.com) their curriculum vitae, list of publications and experience, contact information for three references, a description of their current research, and a brief vision for future objectives and career plans.

Research Projects:
a) Tumor Stem Cell Epigenome: This is a highly collaborative project that is designed to identify breast tumor stem cell-specific histone modification and DNA-methylation patterns and map transcription factor networks that regulate tumor stem cell phenotype.
b) Heat Shock Proteins (HSP): This project is designed to examine regulation of tumor stem cell biology by Heat Shock Proteins (HSP) and its influence on breast cancer phenotype in collaboration with a renowned HSP lab.
c) Development of Culture Media: Our laboratory has specific expertise in developing chemically defined cell culture media specially designed to grow normal and malignant human epithelial and stem cells.
d) Systematic Genotype/Phenotype Correlations: This project is designed to map the oncogenic pathways that cause malignant behavior in genetically engineered malignant mesothelioma cells.
e) Analysis of Cell-of-origin/Oncogene Cooperation: This project is designed to determine the cell origin of different human breast and ovarian carcinomas.

Laboratory environment: The laboratory is located in a highly interactive and highly dynamic department and we collaborate extensively with many renowned experts within and outside Harvard community on specific projects. Our laboratory has extensive expertise in human and mouse Pathology and Pharmacology and has either developed or adapted many of the methods routinely used in the lab including; 1) Highly sophisticated cell-type-specific 2D/3D in vitro tissue culture models, 2) in vivo tumor xenograft models 3) cell type specific chemically-defined media systems, 4) genetically engineered human breast and ovarian cancer cells, and malignant mesotheliomas, 5) analysis of normal and tumor human tissues at the DNA, RNA and protein level. The principal investigator has twenty years of post-graduate basic and translational research experience with expertise in cell and molecular biology, medicine, pathology and pharmacology.

Requirements:
Training Required: PhD, MD/PhD or MD with a solid background in molecular biology and cell biology.
Location and time commitment: Minimum 2 years commitment and ability to re-locate within the US (anticipated summer 2010).
Required Skills: Job Skills: Candidates should have a good command of the English language and should be available for an interview. Competence in basic cell culture and molecular biology methods such as western blots and immunoprecipitation, PCR, Southern blots and Northern blots are essential; experience in FACS isolation of cells is highly desired. Facility with handling mice such as intravenous and orthotopic injections, and necropsy of tumor bearing mice is preferred. Funding guaranteed for one year, subsequent funding will be based on performance, the candidate is expected to write competitive grant applications during this year to fund subsequent years of study.

Relevant References and Publications:
1. Ince TA, et al. Transformation of distinct human breast epithelial cell types leads to different tumor phenotypes. Cancer Cell 2007;12 (2):160-170. 15.
2. Park IH, Zhao R, West JA, Yabuuchi A, Huo H, Ince TA, Lerou PH, Lensch MW, and Daley GQ. Reprogramming of human somatic cells to pluripotency with defined factors. 451:141-6, Nature, 2008.
3. Lerou PH, Yabuuchi A, Huo H, Takeuchi A, Shea J, Cimini T, Ince TA, Ginsburg SE, Racowsky C, and Daley GQ. Human Embryonic Stem Cell Derivation from Poor-Quality Embryos. 26:212-4, Nat Biotechnol. 2008.
4. McAllister SS, Gifford AM, Greiner AL, Kelleher SP, Saelzler MP, Ince TA, Reinhardt F, Harris LN, Hylander BL, Repasky EA, Weinberg RA. Systemic endocrine instigation of indolent tumor growth requires osteopontin. 13;133(6):994-1005, Cell, 2008.
5. Godar S, Ince TA, Bell GW, Feldser D, Donaher JL, Bergh J, Liu A, Miu K, Watnick RS, Reinhardt F, McAllister SS, Jacks T, Weinberg RA. Growth-Inhibitory and Tumor- Suppressive Functions of p53 Depend on Its Repression of CD44 Expression. 11;134(1):62-73. Cell, 2008.
6. Lin MC, Lomo L, Baak JP, Eng C, Ince TA, Crum CP, Mutter GL. Squamous morules are functionally inert elements of premalignant endometrial neoplasia. 22(2):167-74, Mod Pathol, 2009.
7. Elmasri H, Karaaslan C, Teper Y, Ghelfi E, Weng M, Ince TA, Kozakewich H, Bischoff J, Cataltepe S. Fatty acid binding protein 4 is a target of VEGF and a regulator of cell proliferation in endothelial cells. FASEB J. 2009.
8. Chan EM, Ratanasirintrawoot S, Park IH, Manos PD, Loh YH, Huo H, Miller JD, Hartung O, Rho J, Ince TA, Daley GQ, Schlaeger TM. Live cell imaging distinguishes bona fide human iPS cells from partially reprogrammed cells. Nat Biotechnol. 2009 Oct 11.
9. Dinulescu D, Ince TA, Quade BJ, Crowley D and Jacks T. Role of Oncogenic K-RAS in the Development of Endometriosis and Endometrioid Ovarian Adenocarcinoma. Nat Med. 2005;11(1):63-70
10. Team finds way to create cancer stem cells. http://web.mit.edu/newsoffice/2007/breast-cancer-0813.html
11. Research Highlights. On the origins of tumor subtypes. Nature Cancer Reviews, Sept. 2007 http://www.nature.com/nrc/journal/v7/n10/full/nrc2234.html
12. http://www.wi.mit.edu/news/archives/2007/rw_0813.html
13. http://www.bcrfcure.org/action_0708grantees_ince.html
14. http://www.marf.org/Resources/Research/2005Research.html

� Location: Longwood Medical Area, Boston, Massachusetts
� Compensation: According to Brigham and Womens' Hospital Pay scale
� Principals only. Recruiters, please don't contact this job poster.
� Please, no phone calls about this job!
� Please do not contact job poster about other services, products or commercial interests.

Materials Scientist or Chemical Engineering Genius

2009-12-13T11:02:57-05:00
We require a materials scientist or chemical engineering genius to help us develop advanced materials.

Do you have hope for our planet? Do you wish you could be a part of creating our bright, common future? Are you eager to put in many long hours to accomplish our mission, knowing you will receive minimal pay in the short term, with the promise of great financial rewards assuming we are successful?

Have you used CVD, PDV equipment for long enough to know how to get excellent quality materials out of them? Do you know how to modify surfaces and characterize them with a variety of techniques?

Have you set up and run a lab including finding the best equipment at the best price? Can you set it up and use it without any help? When you have assistants, do they share your passion and love working with you?

Are you self motivated and directed? Are you fast and efficient with your time and our money? Do you get along well with others? Are you well organized? Do you love what you do?

Are you a "get �er done" kind of person? Have you been lovingly referred to as a MacGyver?

You must be willing to relocate to a beautiful college mountain town with a small population, fresh air, trees and friendly people, that's only 2 hours away from a major metropolitan area.

If you would like to be a part of our team then send your CV and a cover letter telling us why you belong on our team to IAmTheOne@ambature.com.

Sr. Research Technician & Postdoc (Boston University)

2009-12-12T17:12:54-05:00
The Laboratory of Neural Circuit formation at Boston University is seeking a Sr. Research Technician to lead the development of a new brain-machine interface for studies of neural processing in songbirds.
A Postdoctoral fellowship is also available for the study of the role of sleep in the formation of songbird neural circuits.

3 references and prior work experience in systems neuroscience, or engineering required.

For more information:
http://people.bu.edu/timothyg/Home.html
http://people.bu.edu/timothyg/Home.html

Microfluidics Engineer/MEMS (Medford, Ma)

2009-12-12T14:14:03-05:00
Description: Description of Company:
Nanobiosym is an innovative, young company in Medford, MA founded by an MIT/Harvard alum to work at the interface of nano- and bio- technologies. The company is creating breakthrough scientific insights and revolutionary technologies that emerge from the convergence of physics, nanotechnology, and biomedicine. Nanobiosym (NBS) works symbiotically with its commercial partner Nanobiosym Diagnostics (NBSDx) to discover, develop, and commercialize cutting-edge technologies at this interface. NBSDx is currently developing nanobiotechnology platforms that address global healthcare needs. NBS is a truly exceptional company that has received widespread recognition. This hypergrowth company allows for unique career opportunities with strong long-term incentives.

Duties: Nanobiosym, Inc is seeking strong candidates to work in a dynamic team environment of physicists, engineers, and other scientists. The job responsibility will primarily include developing, designing, characterizing and troubleshooting microfluidics and bio-mems based systems.
Qualifications: Position requirements and skills:
� MS or PhD in Biomedical Engineering, BIO-MEMS, microfluidics engineering or related field with 5+ years relevant post-graduate research experience.
� Extensive hands-on experience required in executing, optimizing and troubleshooting current surface chemistry molecular biology techniques (DNA sequencing, cloning, and mutagenesis).
� In addition to impeccable technical skills, successful candidates possess strong organizational, communication and team skills, and thrive in a fast-paced start-up environment
� Expert proficiency in the use of standard molecular biology techniques (DNA sequencing, PCR, cloning, and mutagenesis).
� Proficiency in use of CAD software and other Bio-MEMS design and simulation software.
� Experience with a wide variety of Fluidic devices (ie flowcells and other microfluidic systems), preferential cell sorting, sample preparation techniques, manipulation and filteration of cells in microfluidic formats.

Personal Qualities:
The ideal applicant will be:
� Excited to work in a hypergrowth company;
� Able to work 6 days/week;
Immediate start date

� Extremely motivated and be willing to work in a fast-paced environment, and hard-working team;
� Committed and enthusiastic about Nanobiosym�s mission and programs;
� Resourceful and flexible;
� Adept at planning, prioritizing, multi-tasking, organizing and following through, while remaining highly energetic and focused;
� Straightforward, self-motivated, and trustworthy;
� Energetic and willing to work hands-on in developing and executing a variety of activities.

RESEARCH ASSISt I / 40 HOURS / DAYS - BWH/ PULMONARY (2196942) ( Boston-On Campus/Longwood Area )

2009-12-11T16:38:21-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ OVERVIEW STATEMENT:
The technician will work with the PI to perform laboratory experiments, including animal experiments, relating to the PI�s projects. The technician will also be responsible for maintaining accurate and concurrent records of experiments performed.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
Duties
1. Performance of laboratory experiments, which include but are not limited to cell culture, molecular biology, and immunostaining (55% time)
2. Routine care for laboratory mice colony (10% time)
3. Maintaining up to date records of the animal experiments (5% time)
4. Performing animal experiments, including cigarette smoke exposures (15% time)
5. Responsible for maintaining detailed records of experiments (10% time)
6. Maintaining inventory of laboratory supplies and assisting with laboratory supply ordering (5% time)
7. Assisting with training and supervising the part-time smoking technicians
8. Additional laboratory duties as needed

QUALIFICATIONS:
Associates degree with relevant laboratory work experience required, BS or BA with relevant laboratory coursework or laboratory work experience preferred. Examples of relevant prior laboratory experience would be work or volunteer experience in a biomedical research laboratory performing RNA extraction, Western blotting, PCR analyses, or cell culture experiments/cell line maintenance. Prior experience with performing experiments with laboratory animals, either through coursework or employment, required.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

1. Excellent oral and written communication skills
2. Excellent organizational skills and ability to prioritize tasks
3. Careful attention to detail
4. Familiarity with computer databases
5. Self-directed learning and ability to work independently
6. Familiarity with basic laboratory protocols

WORKING CONDITIONS:
This day shift job will be performed in a research laboratory and animal facility of an academic hospital. The laboratory is located in the Thorn Building. Basic laboratory equipment and supplies are located either in the laboratory or nearby and is readily accessible during normal working hours.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2196942

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

SR RESEARCH ASSISTANT / 40 HOURS / DAYS - BWH THORACIC SURG (2195652) (Boston-On Campus/Longwood Area)

2009-12-11T16:33:56-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY:
The Clinical Research Associate is responsible for all administrative and operational aspects of clinical research within the Thoracic Surgery Division. He/she monitors patient accrual to surgical trials at the Brigham and Women's Hospital (BWH) and Dana-Farber Cancer Institute (DFCI), including actively recruiting patients on trial, following patients through the protocol treatment program and follow-up, and completing data forms and data management required by the studies.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Responsible for collecting data and maintaining patient information database for studies.
2. Responsible for IRB and other regulatory submissions for protocol submissions and updates, renewals, adverse event reports, deviations, data audits, etc.
3. May be required to do data analysis and run various reports.
4. Interacts with patients/subjects with regard to consenting, data collection, follow-up, and other tasks as assigned. May serves as a liaison between patient and physician.
5. Performs quality control procedures to ensure integrity of data in clinical research database, as determined by Clinical Research Manager.
6. As required, collects biologic samples and specimens and ensures protocol adherence in the operating room, laboratory, and intensive care settings per study guidelines.
7. Answers any phone calls and inquiries regarding clinical research database or study protocol. Refers participants when appropriate to supervisor or clinical staff.
9. All other duties, as assigned.

QUALIFICATIONS:
In order to be eligible for an interview the following skills are necessary: previous clinical work including consenting patients AND basic data management.
Master's Degree preferred.

SKILLS/ABILITIES/COMPETENCIES REQUIRED:
1. Experience using Microsoft Excel, Access and Word are required.
2. Experience using Electronic Medical Records for data collection and review is preferred.
3. Knowledge of statistical software required and experience with SAS and or SQL is preferred.
4. Knowledge of clinical research protocols and clinical trials process, with at least 2 years clinical research experience is preferred.
5. Knowledge of medical terminology.
6. Ability to demonstrate professionalism and respect for subjects rights and individual needs.
7. Excellent interpersonal skills are required for working with the study participants.
8. Careful attention to detail.
9. Good oral and written communication skills.

SUPERVISORY RESPONSIBILITIES:
None

WORKING CONDITIONS:
Data office, operating room, and laboratory working conditions include working under pressure to meet deadlines and meetings, moderate stress.

DRESS CODE:
Professional dress code required.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2195652

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

Cell Culture Scientist/Senior Research Associate Cancer Diagnostics (Waltham )

2009-12-11T15:37:39-05:00
Cell Culture Scientist/Senior Resecrh Associate
www.on-q-ity.com

The ideal candidate will have demonstrated experience with tissue culture on multiple transformed cell lines and/or primary cells. He/she will select cell lines with the desired characteristics, maintain and propagate cell cultures, prepare cell blocks for immunohistochemistry controls and perform cell based assays, cell viability assays, ELISA, western blot, and IHC assays. He/she will clean, sterilize and maintain equipments in the cell culture facility. He/she will develop standard operating procedure for the growth and maintenance of cell lines. In addition, the candidate will maintain good record keeping in notebooks, manage the cell line inventory and database and monitor work to ensure utmost quality and adherence to GLP standards.

The candidate should possess excellent laboratory and data analysis skills, as well as organization, computer software and documentation skills, attention to details, ability to multi-task, excellent time management, and a strong work ethic. Prior experience with cell culture in a fast-paced, high-volume work environment is desirable.

ESSENTIAL KNOWLEDGE, SKILLS & ABILITIES:
�Excellent tissue culture skills
�Strong oral and written communication skills and the ability to work independently in a team environment
�Ability to maintain sterility in the tissue culture facility environment and ability to troubleshoot problems
�Ability to analyze, interpret and present study results and experimental data independently
�Excellent computer software skills
�Ability to work on multiple projects
�The candidate should be self-motivated, reliable, accountable and conscientious in meeting timelines
REQUIRED EXPERIENCE/EDUCATION:
�B.S. or M.S. in cell biology, genetics, molecular biology or related fields
�A minimum of three years prior experience in a cell culture lab
�Prior work experience in pharmaceutical or diagnostics industry desirable

Scientist, Tumor Cell Biology-Biomarker Disc (Waltham )

2009-12-11T15:29:04-05:00
Senior Research Associate/Scientist, Tumor Cell Biology-Biomarker Discovery

On-Q-ity is a biotechnology company creating innovative cancer diagnostics to meet the need for better informing patients and their doctors about cancer care treatment choices.

As a growing personalized medicine company, On-Q-ity is hiring an outstanding individual as a Biomarker Scientist. At On-Q-ity, you will work in the Biomarker Discovery Group to identify, characterize, and implement biomarkers as anti-oncology therapeutic agent predictive tools.. You must have an outstanding working knowledge of cancer cell biology, molecular biology, and imaging technologies. You will play a role in our molecular biomarker discovery efforts and will be carrying out cancer studies with patient specimens.

Candidates for this position will have a B.S. in the Biological or Biomedical Sciences with a minimum of three years of directly relevant experience. Laboratory experimentation is required for this position. Pertinent technical and scientific experiences in the Pharmaceutical/Biotechnology industries are an asset. The Biomarker Scientist will be broadly knowledgeable in translational oncology research, creative, detail-oriented, and highly motivated to contribute to exciting novel directions in personalized medicine.

We are looking for an individual with a strong desire to provide discovery achievements and make a difference through their laboratory work at On-Q-ity.

RESPONSIBILITIES:
Analytical and Problem Solving
�Contribute to tumor cell biomarker discovery utilizing an expert repetoire of technical skills, scientific reasoning, and biomarker strategies with hypothesis-driven experiments.
�Ensure the utmost quality in implementing experiments and interpreting laboratory results.
�Work in a team-oriented environment to discover and validate nucleic acid, protein, and alternative technologies in cancer cell diagnostic applications.
�Use digital imaging and image analysis platforms to analyze biomarkers on patient specimens and pre-clinical model specimens.
�Complete projects from concept through development in a timely manner.
Communication
�Routinely and effectively communicate progress to team members and Research and Development groups in cross-disciplinary and inter-departmental collaborative settings
�Understand and communicate complex hypothesis, concepts, and discovery results
�Contribute a strong sense of responsibility to group progress and corporate culture
ESSENTIAL KNOWLEDGE, SKILLS & ABILITIES:
�Laboratory experience with cancer biology questions and pathway interpretation
�Understanding of biological pathways and the role of protein change in disease states
�Broad background with oncology
�Molecular diagnostics and translational research experiences are beneficial
�Hands-on experience with protein-based biological endpoints in experimentation
�Work effectively in a fast-paced Research and Development team environment with Oncology scientists, pathologists, analysts, and clinicians
REQUIRED EXPERIENCE & EDUCATION:
�A B.S. in a Biological Science or Biomedical Sciences
�Approximately three years experience in the Pharmaceutical/Biotechnology industry is an asset

Sr Digital Imaging Specialist-Innovative Cancer Diagnostics Company (Waltham )

2009-12-11T15:23:39-05:00
Senior Digital Imaging Specialist
www.on-q-ity.com

Comprehensive digital pathology solutions and advanced microscopic imaging systems will be at the core of On-Q-ity's emerging technologies. The ideal candidate will assist in the selection, design, creation, development and implementation of high-performance imaging systems for digital pathology and Circulating Tumor Cell imaging. The successful candidate will utilize expertise in image processing, systems engineering skills, and contribute as a member of a highly collaborative team to work on the infrastructure for image processing and analysis. The ideal candidate should have both a solid practical background (demonstrated by several years of experience developing commercially applications) with extensive experience in image processing. The Imaging Specialist will develop systems and processes related to digital images & image processing. The primary task will require building a scalable clinically imaging system capable of handling significant amounts of data for internal application. The Candidate will actively participate in R&D efforts in developing computer aided image analysis algorithms.

ESSENTIAL KNOWLEDGE, SKILLS & ABILITIES:
�MS or higher degree in physics, engineering, or math, or 5 to 8+ years of equivalent experience with a focus on digital images / image processing and related areas
�Strong skills in image algorithm development and analysis skills
�Medical imaging application experience such as in Radiology or Pathology
�Experience in database design
�Familiarity in Clinical Laboratory Development environment from concept through system deployment with special emphasis on creation of effective workflow processes.
�Proven track record for taking products to market on time & on budget under aggressive schedules

Voice talent for science video and animation (Davis Square)

2009-12-11T15:11:47-05:00
Responsible and reliable voice talent sought for voiceovers on videos depicting laboratory techniques. Applicants should hold an advanced degree in the life sciences or chemistry or have a bachelors with at least 2 years lab experience in these fields. Candidates should be competent with respect to pronunciation of scientific/medical jargon and be able to enunciate clearly. Individuals able to work weekday evenings and weekends will also strongly be considered.

We tentatively plan to hold auditions on 1/09/10, weather permitting. Please reply indicating whether or not you are available on this date.

Chemist: Entry Level Opportunity (Waltham, MA)

2009-12-11T15:02:24-05:00
Job Description:

Our client seeks a contract-to-full time RA to join their research and development efforts. In this position you will run newly developed protocols on HPLC, MS, and LC-MS instrumentation. You will also be involved with developing new methods with the guidance of management. This is an entry level position that will initiate as a contract opportunity and is expected to convert to a full time roll.

Requirements:

BS in Chemistry preferred
Will consider BS Biology and Chemical Engineering candidates that have previous experience utilizing LC-MS
0-2 years of experience utilizing HPLC, Mass Spec, LC-MS, and/or nano-LC-MS
Self motivated individuals that have solid writing and computer skills

Scientist - Tech Support Consultant (Waltham)

2009-12-11T14:18:36-05:00
The Technical Support Consultant provides support to customers and subsidiary personnel on Bio-Rad's molecular biology, protein applications, chromatography, and laboratory imaging products. This includes logging interactions in our service database and providing feedback to management on product problems and needed enhancements. This also includes developing training materials and conducting training.

Education: BS in a life science discipline. MS or PhD a plus.

Experience: 5+ years related experience in a laboratory research setting, industrial R&D group or equivalent. Teaching, service or support experiences a plus. Experience with DNA amplification methods, PCR and real PCR instrumentation and software, protein purification and analysis applications and methods, lab and/or process scale chromatography, or laboratory imaging desired.

Skills: Strong written and verbal communication skills. Expertise in problem-solving, data analysis and troubleshooting instrument and experimental problems. Aptitude for computer hardware and software. Customer service and team player. Ability to act independently of supervision.

APPLY HERE: http://sh.webhire.com/servlet/av/jd?ai=378&ji=2407458&sn=I

Bio-Rad Laboratories, Inc. (NYSE: BIO and BIOb) has remained at the center of scientific discovery for more than 50 years, manufacturing and distributing a broad range of products for the life science research and clinical diagnostic markets. The Company is renowned worldwide among hospitals, universities, major research institutions, as well as biotechnology and pharmaceutical companies for its commitment to quality and customer service. Founded in 1952, Bio-Rad is headquartered in Hercules, California, and serves more than 85,000 research and industry customers worldwide through its global network of operations. For more information, visit www.bio-rad.com.
EOE

Part Time Field Technician (Acton)

2009-12-11T12:58:55-05:00
Assist in the inspection of residential and business properties for mold: carry and set up sample bag and necessary equipment, prepare and label sample media (petri dishes, swabs, test tubes), measure moisture readings, collect and analyze indoor air and surface mold samples, take field notes, send out samples for testing and complete necessary paperwork. Additional duties would include restocking field bags and maintaining equipment.

Requires ability to lift 50lbs. Due to the nature of this position the Field Technician may be asked to collect samples in attics, crawl spaces, etc. Background in construction or biology a plus!

25-30 hours per week. Salary: $15 - $18/hr

Quality Control Technician (Billerica)

2009-12-11T11:19:07-05:00
Position Description: Working in a biotech manufacturing environment, you will report to the Manager of Quality, this individual will work to enhance the company�s focus on Quality.

Job Responsibilities:
� Applies knowledge and application of quality control standards and GMP's
� Accurately maintain batch records and enter data
� Raw material sampling / testing and the associated documentation
� Finished product sampling / testing and the associated documentation.
� Conduct sampling, inspection, and evaluation to ensure that end products comply with specifications
� Interpret quality standards to ensure that all incoming materials comply with requirements
� Routine QC review of plate images and consistency data
� Conducting internal audits
� Perform other duties as assigned, and in accordance with Company guidelines and Standard Operating Procedures

Position Requirements:
� At least 5 years of biotech experience
� A minimum of 2 years clinical lab experience in Quality Assurance/Quality Control including sampling/inspection and/or process monitoring activities
� BA/BS desirable, certificate or 2 year degree required; additional work experience my substitute for formal education
� GMP environment experience a plus
� PC proficiency with Word & Excel
� Interpersonal communication skill (oral and written)
� Should be able handle multiple task simultaneously
� Strong organizational ability and independent
� Detail oriented - accuracy in producing technical reports
� Lab techniques such as ELISA
� Must be able to lift up to 30 lbs

This position is eligible for overtime.

About Aushon BioSystems:
Aushon BioSystems Inc., headquartered in Billerica, MA, provides a comprehensive suite of microarray instruments, consumables and services to leading pharmaceutical, biotechnology, academic and diagnostic clients worldwide. Our unique combination of advanced microarray printing technology, robust biomarker content and innovative multiplex immunoassay development and detection systems delivers exceptional performance, quality and reliability that accelerates pre-clinical and clinical biomarker research.
To learn more visit us at www.aushon.com

Aushon BioSystems is an equal opportunity employer.

Science instructors wanted... teach and tutor the MCAT! $21-24/hr! (BU, BC, Tufts, Harvard, Northeastern)

2009-12-11T11:15:25-05:00
The Princeton Review is seeking energetic men and women who have backgrounds in the humanities or hard sciences to teach our Medical College Admissions Test (or MCAT) prep courses in and around Greater Boston!

Trainings are coming up in the forthcoming weeks for the following test types:

MCAT Physics training dates: Fri, January 15th (eve. only), January 16th-17th (full days) (possible December training dates TBD)
MCAT General Chemistry training dates: Fri, January 15th (eve. only), January 16th-17th (full days) (possible December training dates TBD)
MCAT Organic Chemistry training dates: Fri, January 15th (eve. only), January 16th-17th (full days)
MCAT Biology training dates: Fri, January 15th (eve. only), January 16th-17th (full days) (possible December training dates TBD)

The Princeton Review is the dominant global force in test prep. We have recently revamped our compensation policies to provide teachers with more support than ever before, including but not limited to higher starting wages and raise opportunities, paid training and preparation time, excellent travel reimbursement policies, part-time medical, dental, and life insurance, and a competent full-time staff, many of whom are teachers themselves. We pride ourselves on the superior quality of our product - and that product begins and ends with YOU! Here's how to get involved:

1. Register. Let us know you�re interested by filling out our online application or by emailing ChrisJ@review.com directly. You may also call us at 617-558-2828 to speak with a local representative.

2. Audition. We will invite you to one of several local group teaching auditions, where we will quiz you on relevant material and ask you and other prospective instructors to present on a topic of your choosing for 5 minutes at a time. Auditions will be run several times per month in multiple locations, such as Newton, Boston, Worcester, Concord (NH) and Providence (RI). At this group interview, you will have the opportunity to learn about the job itself and ask questions pertinent to your role in the company.

3. Train. Once approved by your audition leader, you may train for any subject in which you have a background or proclivity. Our most immediate trainings are filling up fast! We are always accepting applications for other subject types as well, including GMAT, GRE, LSAT, and SAT.Trainings are often held out of our Newton, MA office, so appropriate transportation is required; we can often host out-of-state residents at local hotels.

4. Start teaching! A new SAT teacher will generally teach one or two nights per week, or about 4-10 hours. (Those who want more work, however, usually get it!). Classes are run in and around the Boston area, with particular attention paid to BU, Harvard, MIT, Tufts, Northeastern, and BC.

If you�re eager to start right away, please contact Chris Jacobs at 617-558-2828 or ChrisJ@review.com with your resume and test results; if you've chosen to use our online recruiting system, the information will come automatically. Start the process now and you can be teaching in just a short time! Best of luck!!

RA Microbiology needed ASAP (Greater Boston)

2009-12-11T09:54:32-05:00
ADANTE STAFFING

Our client has an immediate need for a Microbiology Research Associate. The ideal candidate will have hands-on experience in basic microbiology techniques, data recording and analysis, and be a team player able to multitask in a fast-paced startup environment. Superior organizational skills required along with a strong desire to work in positive, constructive and high energy environment.

Responsibilities:
Evaluate antimicrobial properties of standard industry coatings and surface architectures through bacterial adhesion, flow cell, and radiolabel testing.
Assist in design of novel assays to evaluate antimicrobial and antithrombotic properties of leaching and non-leaching material samples.
Collaborate with our world class chemistry team in preparation of material samples.

Requirements:
Minimum bachelors in microbiology or biological engineering
Experience with sterile technique, and microbiological assay execution and documentation

This position is scheduled for a Thursday through Monday 1st shift.
Local candidates only! Sponsorship is not available for this role.

Interested candidates should send an updated resume in MS Word format to stone@adantestaffing.com

www.adantestaffing.com

Scientific Associate II (Cambridge, MA)

2009-12-11T02:53:01-05:00
Work with development teams to make significant contribution to molecular diagnostic research and development projects.

Major responsibilities include but not limited to:
1) Grow and archive cells for the development group with good quality in a timely manner.
2) Independently execute experiments with good quality in support of molecular diagnostic development, including sample prep, quantitation of gene expression, sequencing, reagent QC and etc. Pay attention to details, and is capable of effective troubleshooting.
3) Monitor and order lab supplies. Maintain tissue culture lab in compliance with company�s policy, GLP and HSE guidelines.
4) Design experiments with moderate guidance.
5) Keep detailed record on lab notebooks, reagents, and maintenance of lab equipments.
6) Be willing to learn new techniques and continue to gain scientific knowledge. Participate in project meetings, present data, and provide technical input.

The candidate must have a BS/MS degree in Life sciences (such as Molecular and Cell Biology, Genetics and Biochemistry) with at least three years of industrial experience.
* 1-3 years of lab experience in tissue culture. Working experience with a broad range of different cell types is required.
* Hands-on experience in sample preparation, nucleic acid detection (such as PCR, sequencing), automated liquid handling and assay development.
* Familiarity with GLP environment, documentation and quality system is highly desirable but not required.
* Good communication and time management skills.

In order to be successful in this position, the candidate should be a good team player in multidisciplinary environment, capable of multiple tasking, and able to be fully committed to development timelines.

To Apply for this position, please CLICK HERE

Group Leader- Antibody Engineering-0900481 (Rockland, MA)

2009-12-10T17:52:41-05:00
At EMD Serono, Inc. our strength is our people!
About the Company

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.

Description
EMD Serono is seeking to appoint a motivated and well qualified scientist for the Protein Engineering and Monoclonal Antibody Technologies (PEAT) group within New Biological Entities (NBE) Technologies. He/she will be responsible for the Monoclonal Antibody Engineering needs of the group and head up a laboratory staff of three with a potential to grow.
This individual will report to the Head of PEAT at their facility in suburban Boston and will be part of an energetic team in a key strategic area of the Discovery organization within EMD Serono. In this regard, he/she will play an important role in the overall responsibility of NBE Technologies for the discovery, optimization and progression of the Company's biotherapeutics discovery pipeline.
As Scientist - Antibody Engineering the incumbent will have responsibilities including, but not limited to, the following:
Leading a group of scientist and technicians in the Monoclonal Antibody Engineering laboratory
Assuming responsibility for the humanization and optimization of antibody candidates generated by hybridoma- or phage display-technology.
Managing the group and taking responsibility for its projects by driving and coordinating his/her direct reports in achieving the specific objectives of the respective research projects.
Advancing antibody technologies within his/her own group as well as influencing the strategies on current and future technologies.
Representing the monoclonal antibody department in specific antibody project teams.
Taking responsibility for defining requirements for research projects and identifying potential constraints and risks.
Use of problem solving skills in evaluating issues, and monitoring and initiating corrective actions where necessary.
Taking responsibility for proposing new projects or amendments to existing projects to the Head of PEAT in the US.

Qualifications
The ideal candidate will have a Ph.D. in molecular biology, biochemistry, biotechnology or biological sciences.
This individual will be a highly motivated scientist with a proven track record in antibody engineering and must have several years of post-doctoral experience in an academic or industry setting.
A strong background in molecular biology, with extensive experience in antibody engineering, antibody expression and purification, and biochemical and biophysical methods for the analysis of antibodies is required. An interest to work part-time at the laboratory bench is desirable.
Familiarity with antibody phage display technology and affinity maturation, and interpretation of computational modelling of antibody-antigen interactions would be useful. Further, experience in preclinical development of therapeutic antibodies is desirable.
It is desired that the candidate demonstrate an aptitude to interact constructively with others across multiple cultural backgrounds in a dynamic matrix structure. He/she must have the ability to collaborate with colleagues throughout the organization in research functions i.e., bio-informatics, protein and cell sciences and structural biology and in corporate functions i.e., business development, intellectual property.
Further to this the candidate will possess strong communication skills, both oral and written. He/she should be confident in presentation with parties both small and large.
As leader of a group, the candidate must be committed to its members and foster a teamwork approach. This will partially be accomplished through the facilitation of a positive work environment. He/she should be skilled in motivating and coaching others as well as interacting well in a team.
The candidate will be, above all, a proactive self-starter with a positive "can do" attitude. He/she will have demonstrated success in achieving goals, be strongly results oriented and have the ability to drive tasks through to completion.
The incumbent will be required to focus on multiple issues at one time, and must have the ability to organise and direct diverse activities in a changing environment, often under time pressure.
With a mature, self-confident and well-balanced personality, it is essential that the candidate also possess a high standard of ethical and intellectual integrity.
Finally, the candidate must be strongly computer literate.

Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0900481

EMD Serono, Inc. Named as a Top Employer by Science Magazine
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Senior Statistical Programmer-0901356 (Rockland, MA)

2009-12-10T17:11:03-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
Independently program (or write validation programs for) and document tables/listings/graphs for clinical trials or portions of clinical trials requiring routine data manipulation and analysis.
Routine data manipulation and analysis with limited direction.
Program (or write validation programs for) and document tables/listings/graphs for clinical trials requiring complex data manipulation and analysis.
Provide input into general standardization efforts and create (or validate) global macros that streamline repetitive operations.
Mentor biostatisticians and statistical programmer/analysts with advance SAS programming techniques.
Interface with SAS technical support to resolve software problems.
Coordinate, validate and implement SAS upgrades and licenses.
Independently provide input into CRF specifications to collect data specified in the protocol and query with SAS technical support to resolve software problems, coordinate, validate and implement SAS upgrades and licenses.
Independently provide input into CRF specifications to collect data specified in the protocol and query check specifications and provide input into analysis plan specifications and data presentations for clinical trials requiring complex data manipulation and analysis.
Independently program (or write validation programs for) patient randomizations.
Independently create (or validate) non-standard complex derived datasets.
Create project and study phase sub-directories ensuring that all project work resides in the correct project and study phase sub-directories.
Validate study phase flags in oracle tables and download study phase records from oracle tables to create analysis datasets.
Audit changes to the database between study phases.
Understand and follow all statistical and statistical programming SOP�s as well as any other relevant SOP.
Lead process improvement teams as required.
Effectively communicate analysis specification and programming/data issues that arise prior to or during analysis in a timely manner.
Professional Skills & Experience
MS, BS (or equivalent).
6 years pharmaceutical/biotech or other relevant experience.
Fundamental knowledge of relevant statistical areas.
Fundamental knowledge of relevant clinical areas.
Advanced knowledge of SAS/Bas, SAS/STAT; knowledge of SAS/Connect, SAS/Macro, SQL.
Excellent communication skills
Ability to independently solve complex problems logically.
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0901356

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Principal Biostatistician-0901059 (Rockland, MA)

2009-12-10T16:47:20-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
Function as a project biostatistician coordinating statistical aspects across clinical trials within a specific project in a therapeutic area
With limited direction, provide statistical input for statistically complex protocol development
With limited direction, write statistical analysis plans and perform statistical analyses for statistically complex clinical trials
With limited direction, write statistical analysis plans and perform statistical analyses for safety and efficacy summaries for regulatory submissions
Independently provide statistical input for statistically routine protocol development
Independently write statistical analysis plans and perform statistical analyses for statistically routine clinical trials
Participate in departmental standardization efforts
Provide support towards statistical research
Key Tasks & Responsibilities
Participate on clinical development teams
Provide statistical input into clinical development plans
With limited direction, participate in the development of statistical standards for clinical development programs
Review statistical analysis plans written by other statisticians on the project
Review statistical analysis results produced by other statisticians on the project
Review statistical methods sections and the interpretation of results written by other statisticians on the project
Provide statistical support for manuscripts and review manuscripts for accurate statistical interpretation
Functional Roles and Responsibilities:
With limited direction, provide statistical input for protocol/CRF development (e.g., trial design; sample size estimation for the most efficient and practical design; patient randomization; accurate, logical, clear, concise and thorough evaluation of results section; effective CRF specifications to collect data specified the protocol)
With limited direction, write statistical analysis plans for clinical trials as well as for integrated safety and efficacy summaries. Analysis plans written include the most appropriate statistical methodology and data presentations.
With limited direction, analyze clinical trials
With limited direction, write accurate, logical, clear, concise, thorough and objective statistical methods sections for clinical trial reports
Review and co-author clinical trial reports ensuring the accuracy of the statistical interpretation
Understand and follow all Global Biostatistics WIs/SOP as well as any other relevant WIs/SOPs. Provide input into all newly developed departmental quality documents
Provide input into general standardization efforts (e.g., CRFs, query checks, statistical methodology, standard statistical programs, data presentations)
With direction, interact with regulatory agencies regarding statistical issues
With direction, develop responses to regulatory agency requests that maintain perspective and are within the appropriate context
Participate effectively on clinical trial teams
With direction, provide solutions for complex issues presenting alternatives and identifying the best solution
With limited direction, communicate routine and complex statistical concepts and results to non-statistical internal and external colleagues in a clear, concise, focused and articulate manner
With limited direction, function as the statistical primary contact with CROs for studies that are outsourced, and ensure the accuracy and timeliness of the CROs analysis alerting management to any unforeseen circumstances
Produce assigned work within the timelines provided ensuring deadlines are met
Education/Languages
Ph.D. or MS in statistics, biostatistics or related discipline
Fluent in English (French or German is a plus)
Professional Skills & Experience
Several years experience in the Pharmaceutical/Biotechnology industry
Working SAS knowledge and proficient in SAS/Stat
Knowledge of ICH Statistical and Clinical Report Guidelines
Familiarization with relevant therapeutic areas
Personal Skills & Competencies
Ability to work in a matrix organization
Ability to work with multi-disciplinary groups
Strong communication, negotiation and issue resolution skills
Balance concurrent tasks and responsibilities
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0901059

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

Core Lab Technician, Dept of Medicine/Genetics Program (Boston University School of Medicine)

2009-12-10T14:16:15-05:00

Perform a variety of molecular genetics laboratory services including extraction of DNA/RNA from a variety of clinical samples, florescent DNA sequencing and genotyping, utilization of robotic liquid handling stations, and establishing lymphocyte cell lines. Design primers and optimize PCR based assays. Responsibilities are evenly divided between all aspects of laboratory operations and training for specific tasks will be provided by the laboratory. A successful candidate should be able to work both independently and on a tem and have excellent interpersonal skills.

Required skills: Bachelor�s degree in the sciences with some relevant experience required. Computer literacy is desirable.

This is a full time permanent position.

Grade level is 24 (Rates increase in January)

Please note job posting #5103 on your cover letter and mention you saw this on Craigslist.

BU has great benefits!!

Senior Scientist Cancer Cell Biology at Innovative Diagnostics Compay (Waltham )

2009-12-10T13:52:33-05:00

Senior Scientist, Cancer Cell Biology

As a growing personalized medicine company, On-Q-ity is seeking to hire an outstanding individual in the capacity of Senior Scientist. At On-Q-ity, you will work as a team member in Cancer Cell Processing and Characterization. This scientific team is committed to perfecting a microfluidics cancer cell detection device, requiring state-of-the-art cancer cell capture and biomarker technologies. You must have an outstanding working knowledge of cancer cell biology, molecular biology, and imaging technologies. In this capacity, you will be responsible for implementing cancer cell processing and molecular biomarker discovery.

Candidates for this position will have a Ph.D. in the Biological or Biomedical Engineering Sciences with a minimum of three years of directly relevant experience. Laboratory experimentation is required for this position. Pertinent oncology, technical, and scientific experiences in the Pharmaceutical/Biotechnology industries are an asset. The Senior Scientist will be broadly knowledgeable in translational oncology research, creative, detail-oriented, and highly motivated to contribute to exciting novel directions in personalized medicine. We are looking for an individual with a strong desire to make a difference through their discoveries and scientific insights at On-Q-ity.

RESPONSIBILITIES:
Analytical and Problem Solving
�Contribute to circulating tumor cell biomarker discovery and development utilizing a broad oncology understanding, pathway logic, bioinformatic, and computational strategies in hypothesis-generating experiments
�Design experiments and monitor laboratory results for patient specimens and pre-clinical models
�Discover and validate nucleic acid and protein biomarkers in cancer cell diagnostic applications
�Ensure the utmost quality by superior experimental design, implementation, and interpretation
�Lead projects from concept through development to completion in a timely manner
�Utilize full understanding of biological mechanism and their interactions in cancer
�Apply creative thinking towards discovering non-obvious clinical applications of biomarker trends
Communication
�Work effectively in a fast-paced Research and Development team environment with Oncology scientists, analysts, and clinicians
�Propose and successfully meet Project-based timelines and milestones
�Lead collaborative interpretation of biomarker results engaging scientific and clinical perspectives
�Routinely and effectively communicates progress to members of Research and Development teams as well as executives, scientific/clinical advisory boards, and collaborators
�Explain complex hypothesis, concepts, and discovery results internally and publicly
�Exercise a strong sense of responsibility to group progress, integrating data-driven concepts with clinical need
Managerial
�Direct activities for a small team defining new approaches for cancer monitoring
�Lead focused project teams on cancer patient discovery and validation studies
�Participate in key pharmaceutical partnerships
�Represent Discovery and Project team activities to management on routine basis
ESSENTIAL KNOWLEDGE, SKILLS & ABILITIES:
�Laboratory experience with cancer biology questions and pathway interpretation
�Understanding of biological pathways and the role of protein change in disease states
�Broad background with oncology
�Molecular diagnostics and translational research experiences are beneficial
�Hands-on experience with protein-based biological endpoints in experimentation
REQUIRED EXPERIENCE & EDUCATION:
�Experience with rare cell detection and fluorescence microscopy is a plus
�A Ph.D. in a Biological Science or Biomedical Engineering
�Relevant experience in the Pharmaceutical/Biotechnology industry is an asset

Laboratory Operations manager at Innovative Diagnostics Company (Waltham )

2009-12-10T13:46:51-05:00

Laboratory Operations Manager

The Laboratory Operations Manager is responsible for the general oversight of the research and development laboratories to ensure smooth and efficient functioning and operation. The Laboratory Operations Manager will create, establish and implement procedures and guidelines pertaining to facilities, equipments, personnel, methods, processes, records, controls, SOPs, final reports (for data integrity), and archives in compliance with good laboratory practices. The Manager will also oversee safety and environmental health program and will participate in facilities management. Ideally, this successful candidate will assist in the establishment of Quality Assurance programs and documentation for the Development and Research Departments.

The high complexity nature of the work requires thorough knowledge of GLP and EH&S, excellent attention to detail, effective written and verbal communication skills, the ability to multi-task and be flexible with tasks and schedules, and the ability to work independently in a team environment.

RESPONSIBILITIES:
�Establish practices and guidelines to assure laboratories function in a manner consistent with good laboratory practices
�Initiates quality-control measures and monitors for compliance with laboratory standard.
�Participate in quality assurance activities
�Recommends procurement of new laboratory equipment and installs, monitors and oversees maintenance/repair needs of laboratory equipment.
�Trains company personnel in and communicates regulatory compliance.
�Coordinate sample procurement with counterpart clinical centers, pharmaceutical companies, biotechnology partners and other institutions for exchange of samples, technology sharing, information, and collaboration.
ESSENTIAL KNOWLEDGE, SKILLS & ABILITIES:
�BS and five or more years of experience in high volume, high complexity Clinical Laboratory testing environment preferred, supervisory experience desirable.
�Advanced degree preferred.
�Exhibit leadership skills such as good judgment, sound analysis and decision making, effective interpersonal skills, and the ability to effectively communicate across all levels of the laboratory and across departments

Laboratory Supervisor at Innovative Cancer Diagnostics Company (Waltham Ma)

2009-12-10T13:39:12-05:00

Laboratory Supervisor
Posted: 11/16/09
As a growing personalized medicine company, On-Q-ity will be hiring an outstanding individual in the capacity of Laboratory Supervisor. You will work in a laboratory group focused on manufacturing of a cancer cell capture device, the processing of cancer specimens, and their analysis ex vivo. The position requires previous laboratory experience and a high level of multitasking and coordination with external partners. You will need to be highly skilled at coordinating, supervising, and monitoring laboratory activities on a day-to-day basis and will work with management to ensure smooth and efficient functioning of the laboratory processes, specifications, storage and shipping, quality control, and data analysis.

RESPONSIBILITIES:
�Oversees staff and activities of the laboratory; determines priorities; schedules procedures, assigns and distributes work
�Coordinate with counterpart clinical centers, pharmaceutical companies, service providers, biotechnology partners and/or customers, and other institutions for exchange of samples, technology sharing, information, and collaboration
�Performs advanced or specialized tests and other related laboratory techniques. May duplicate work of others to confirm test results. Re-evaluates methodology, makes recommended changes, and assists in test interpretation. Determines if further testing should be done on blood samples or if test should be repeated.
�Initiates quality-control measures and monitors work quality for compliance with laboratory standards
�Completes Standard Operating Protocols and special projects, such as studies, inventories, research reports, etc.
�Responsible for purchasing supplies for laboratory. Recommends procurement of new laboratory equipment and monitors maintenance/repair needs of existing equipment
COMMUNICATION:
�Work effectively in a fast-paced Research and Development team environment with Oncology scientists, analysts, engineers, and clinicians
KNOWLEDGE, SKILLS & ABILITIES:
�Four to six years' experience in a laboratory environment with similar functions
�Expert ability to organize and coordinate diverse activities
�Demonstrated supervisory, communication, management and motivational strengths
EDUCATION AND EXPERIENCE:
�Four years' appropriate college degree in science, or equivalent.

Scientific Associate (Boston)

2009-12-10T11:10:43-05:00

Immediate opening for a Scientific Associate I to help explore the regulation of signaling pathways in ocular surface tissue epithelial cells. Minimum requirements include a Master�s Degree, or equivalent, as well as 5 to 6 years experience with cell culture, protein and molecular biological techniques. Proficiency with lipid biochemical methods and computers will be extremely helpful. Salary for this position will be commensurate with experience, not to exceed $65,000 with benefits. Please send resume, with cover letter and the names of 3 references to: email: frances.ng@schepens.harvard.edu or Schepens Eye Research Institute, Human Resources Department, 20 Staniford Street, Boston, MA 02114. We are an Equal Opportunity/Affirmative Action Employer. M/F/H/V.

Sr. Research Associate: In Vivo (Cambridge)

2009-12-10T10:25:15-05:00

Required Skills

� Strong hands-on animal handling and dosing skills with mice and rats (various routes of injections, restraining techniques, anesthesia, small surgeries, animal monitoring). Experience in applying in vivo models for drug discovery and efficacy testing of treatments for immunological diseases.
� Ability to perform and possibly to develop or improve in vivo models for inflammatory and autoimmune diseases
� Perform translational studies for immune parameters: Sample collection and preparation, analysis by ELISA assays, cell based assays such as flow cytometry
� Plan, execute, analyze, and report experiments
� Strong communication, documentation, and writing skills
� Capacity to work independently with minimal supervision in executing outlined studies
� Ability to multitask and to meet timelines while handling multiple studies and competing priorities

Required Experience

BS or MS degree in a related scientific discipline with of 2 to 5 years of industry experience
� Hands-on experience with running in vivo studies in animal models of inflammation and/or autoimmune diseases
� Working knowledge in immunology
� Experience in biomarker assessment and sample analysis is highly desired
� Experience in oncology models is a plus

Email resume as a word document to: jobs@cwsciences.com

Commonwealth Sciences, Inc.
http://www.cwsciences.com

Protein Chemist, recombinant proteins for drug discovery (Cambridge)

2009-12-10T10:07:32-05:00

Sirtris, a GSK Company, and 2009 winner of American Business Awards Best Overall Company of the Year and Scrip Award winner of Best Biotech Company of the Year�Xup to 70 employees, is developing small molecule drugs that target the sirtuins, a recently discovered family of seven enzymes associated with diseases of ageing. Modulation of these enzymes offers the promise of drug discovery in multiple therapeutic areas.

Lead the production of recombinant proteins for drug discovery

Join an enthusiastic team in a growing drug discovery company. Sirtris is seeking a scientist to produce known and novel proteins to be used in lead discovery, structural studies and other activities related to drug discovery.

Primary responsibilities for this position are to:

Establish a credible and sustainable capability for the production of recombinant proteins
Be dedicated to hands on laboratory work with responsibility for the production of recombinant proteins
Manage protein production at contract research organizations (CRO��s)

BS/MS/PhD with 5+ years of post graduate experience preferably in industry and demonstrable expertise in all aspects in the production of recombinant proteins including cloning, expression, and purification, from bacterial and eukaryotic systems. Requires expertise in the use of contemporary techniques for protein purification including the use of AKTA or equivalent systems in addition to more classical chromatographic methodologies. Prior experience in mutagenesis, structural biology and/or enzymology while not essential would be preferred.. A successful candidate will work independently under general direction in a fast-paced environment. Demonstrated managerial experience of CRO or other external contractors is strongly preferred. Qualified candidates will have strong oral and written communication skills.

Join Sirtris where we are creating revolutionary medicines for diseases of aging. We hope you will see this as a unique opportunity to work in a fun, collaborative, and creative environment with leading edge science.

To apply, please go to: http://sirtrispharma.com/careers.html

Sirtris, a GSK Company, 200 Technology Square, Cambridge, MA 02139

Sirtris will only accept job applications from candidates who are properly documented with authorization to work in the United States.

Note to Employment Agencies: Please do not forward any agency resumes. Sirtris is not responsible for any fees related to resumes that are unsolicited.

Health Science Specialist/Research Laboratory Assistant (West Roxbury, MA)

2009-12-09T17:31:18-05:00
Gastroenterology research laboratory affiliated with Harvard Medical School and VA Boston Healthcare System seeks motivated individual to work as laboratory assistant at West Roxbury division of VABHS, and funded by a grant from the Boston VA Research Institute, Inc. (BVARI), founded in 1990 to conduct, promote and support the medical research and education activities of the VA Boston Healthcare System and to advance the well being of veterans and the general public by these endeavors. This position is working on animal model stem cells for possible cell replacement and gene delivery in the gastrointestinal tract. Another clinical project involves a novel endoscopic imaging device for detection of lesions of the GI tract. Major duties include performance cell culture, molecular biology techniques and histology experimentation. Assistance with animal experimentation will also be done. Training will be provided for specialized techniques as necessary. Good computer and communication skills and biological knowledge are required. This is a good position for individual interested in eventual continuation to medical or graduate training. If you have these technical and research skills and are interested in applying for this position please send your cover letter and resume to Hiroshi Mashimo M.D., Ph.D. hmashimo@hms.harvard.edu.

Associate Marketing Communications Manager (North Billerica MA)

2009-12-09T14:07:08-05:00
This is a unique opportunity to join our marketing team and take part in the launch and rapid growth of enabling new technology and products for biotech, pharma and academic customers worldwide.

Position Summary
As an integral part of the Marketing team, you will develop the �voice of the customer� for Seahorse products, facilitate development of clear, strong, and persuasive technical content for all marketing programs, and ensure that Seahorse products and technologies are positioned effectively in all market segments and regions.

Key Responsibilities:
- Create technical sales and market development tools
- Develop messages & tools that communicate the value of Seahorse technology to specific market segments and regions
- Write content for web, print, social media, PR
- Utilize multi-media and other web-based strategies to communicate message and to drive traffic to web and educate end user about product value.
- Determine and manage trade shows/events appropriate for Seahorse technologies
- Ensure alignment, consistency, and integration of key communication elements in all communication campaigns.
- Prioritize and manage projects as well as develop, maintain and track budgets.
- Build effective working relationships with all internal and external stakeholders.

Qualifications
- BA or BS in a life science
- 3+ years related experience, with at least 1 year experience in the Life Science market
- Knowledge of/ability to learn, understand and discuss basic cellular biological processes
- Ability to translate new enabling technologies into easily understood copy or script that generates results.
- Excellent writing, editing, proofing and verbal communication skills to write and correct copy and express ideas to others.
- Strong organizational, project, and time management skills.
- Ability to work independently
- Comfortable working in a matrix management environment
- Experience in a biotech or start-up experience a plus
- Familiarity with salesforce.com a plus

The Company:
Founded in 2001, Seahorse Bioscience designs and manufactures analytical instruments, bioprocessing systems, and consumables for the Life Sciences. Seahorse products are changing cancer, aging, obesity and diabetes drug discovery programs the world over. Headquartered 30 miles north of Boston, in North Billerica, Massachusetts, Seahorse Bioscience maintains software development in Seattle, Washington and manufacturing in Chicopee, Massachusetts. Our products can be viewed at www.seahorsebio.com.

Category Manager, Commercial/Marketing (Biopharmaceutical) 0901373 (Rockland, MA)

2009-12-08T21:02:28-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
The Category Manager is responsible for managing a portfolio of Commercial/Marketing spend categories within a bio-pharmaceutical organization. As a key link between internal customer departments, Procurement, and EMD Serono's external supplier base, the Category Manager is accountable for understanding key business drivers and ensuring that customer requirements are fulfilled. Extensive cross-functional collaboration, and use of strategic sourcing best practices are keys to maximizing value in terms of cost savings/avoidance, risk reduction, quality and supplier performance. The role holder conducts internal and external spend and market analyses, identifies opportunities, develops category strategies, leads sourcing teams, negotiates contracts and manages key supplier relationships. The role holder is an energetic, flexible team player capable of forming strong relationships throughout the entire organization, in addition to successfully leveraging resources, processes and tools to achieve desired outcomes.
KEY TASKS AND RESPONSIBILITIES
Actively work with the business partners to source goods and services in accordance with policies and procedures.
Develop subject matter expertise in order to enhance ability to add value from a procurement perspective.
Ensure the timely execution and delivery of products and services in accordance with business timelines.
Drive value, service and cost savings through optimum vendor selection, management and effective negotiation.
Lead the supplier performance management process for assigned categories.
Provide strategic insight and access to all relevant spend and related data.
Ensure that the business area engages and fully supports the supply base and supplier management strategies that impact their business area.
SKILLS & COMPETENCIES
Willing to diplomatically challenge concepts and tackle large, complex tasks.
Active external learner - can identify new and better ways, and takes advantage of ideas, best practices and solutions
Ability to support/lead and affect transformational change effort
Customer focus and successful management of many internal customers and competing priorities and the need to continually allocate and balance resources across projects, or Account Planning
Strong skills in strategic influencing, collaboration, communications, and conflict management
Strong spend and supplier analysis skills
Qualifications
EDUCATION/PROFESSIONAL EXPERIENCE
Bachelor's degree required (Master's degree preferred)
8 years of relevant work experience with strong preference in a large multi-national bio-pharmaceutical organization
At least 5 years experience in strategic sourcing/category management, conducting cross-functional sourcing projects and negotiating contracts for complex services, Project background in most, if not all, key categories of bio-pharmaceutical commercial spend (i.e., Agency, Media, Market Research, Medical Education, Conferences, Print, Premiums and Direct Marketing)
Strategy development experience
C.P.M. or CPIM certificate preferred
EMD Serono 0901373

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Toxicologist-0900910 (Billerica, MA)

2009-12-08T20:49:30-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
The representative of Toxicology at the R&D hub in Billerica, MA, USA, serves as the interface between discovery teams and the global safety function. He/she represents toxicology on those teams and ensures high quality drug candidates in respect to their non-clinical safety profile. He/she also supports development projects with focus on the USA.
Functional Tasks
Serve as the interface between discovery teams at the R&D hub in Billerica and the global toxicology function
Support discovery activities with high quality toxicology input
Support development activities for compounds with focus in the USA with toxicology expertise
Prepare internal and external (e.g. IND) documents supporting the advancement of drug candidates in the pipeline
Participate in and contribute to internal and external meetings related to drug candidate discovery and development
Education/Languages
DVM, MD, PhD in a life science field, or comparable education
DABT or eligible for DABT status, or comparable certification
English (oral and writing), German desirable
Professional Skills & Competencies
Profound knowledge and expertise in pharmaceutical compound (NCE and NBE) toxicology and non-clinical safety assessment in general
Experience in early toxicological assessment and testing of drug candidates
Knowledge and experience in drug development with special emphasis on non-clinical safety
Personal Skills & Competencies
Teamwork
Strong teamwork skills are essential as the major focus of the position is working in and with teams
Customer Orientation
Relates to internal customers, e.g. discovery teams, development functions, and external customers, e.g. FDA
Communication with Impact
Excellent communication skills and a high level of persuasive power backed by excellent scientific expertise are required for dealing with both internal and external customers
Strategic Orientation
Being located at an R&D hub with, however, the major parts of the own organization located on a different continent requires a deep understanding of strategic necessities in a global organization
Change and Innovation
Discovery project support in particular requires innovative approaches with case by case tailored assessment packages
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0900910

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

MGH/Harvard/MIT Health Systems Research for Undergrad Winter Recess+ (Cambridge)

2009-12-08T19:37:05-05:00

Scientist: Protein Formulation (Cambridge)

2009-12-08T14:32:27-05:00

As part of the Analytical and Formulation Development group, the individual will lead the formulation development efforts to support pre-clinical through early clinical development. The individual will work closely with the process team and will be an integral part of Product Development, responsible for the pre-formulation and characterization of our drug candidates. The individual will also interact and collaborate with other formulation scientists from the parent company organization.

Responsibilities:
� Lead formulation development efforts for early phase drug candidates.
� Participate in the process development activities of the drug candidates.
� Participate in analytical method development, particularly for stability indicating methods.
� Design and set up stability and stress studies for formulation development; compile, interpret and present results in a concise fashion.
� Characterize formulations in development using appropriate biophysical techniques; compile, interpret and present results in a concise fashion.
� Make recommendations to the senior CMC team on the formulation candidates for our molecules based on data generated from stability studies and characterization.

Requirements:
� Ph.D. in Pharmaceutical Sciences or relevant discipline, with 2 to 5 years of post-doctoral experience in protein formulation, preferably in an industrial setting. Candidates without PhDs but commensurate industrial experience will also be considered.
� Solid knowledge in protein biochemistry and analytical chemistry is essential. Strong hands-on experience with analytical instrumentation (HPLC, electrophoresis) and protein characterization techniques (mass spectrometry, DSC, fluorescence) is critical.
� A demonstrated track record in liquid formulation development for proteins is necessary. Knowledge in lyophilized formulation development is desirable but not essential.
� Current knowledge with IP issues and industry practice/regulatory guidelines on protein formulation and is essential.
� Enthusiasm, willingness to learn, strong work ethic, broad scientific interests and ability to work on multiple projects simultaneously.
� Excellent organizational skills are required, along with demonstrated initiative-taking and innovative thinking within a team environment.
� Excellent interpersonal and communication skills along with the willingness to collaborate within and outside of the team.
� Embrace our core values: Challenge ourselves to excel; Seek and act to achieve the best outcome; Make and keep commitments; Create extraordinary experiences.

Commonwealth Sciences, Inc.
http://www.cwsciences.com

Research Fellow (Boston)

2009-12-08T14:17:56-05:00

The Schepens Eye Research Institute, an affiliate of Harvard Medical School, has an immediate opening for a Postdoctoral Fellow to study the role of cell surface proteins (mucins and galectins) in mucosal barrier function. The project involves biochemical methodology such as protein purification and enzymatic analysis, in addition to surface plasmon resonance and siRNA technology. Candidates should have experience in biochemistry or molecular biology with a good publication record and strong credentials. A solid background in carbohydrate chemistry is desirable.

Submit CV, along with three reference names, to: The Schepens Eye Research Institute, Harvard Medical School, attn: Dr. Pablo Arg�eso, 20 Staniford Street, Boston, MA 02114 or email pablo.argueso@schepens.harvard.edu.

Visit our site http://www.theschepens.org/ for more information about the Institute. The Institute is an equal opportunity/affirmative action employer.

QA Specialist (Boston)

2009-12-08T13:51:32-05:00

Validation Professionals, Inc. is a validation and compliance consulting company serving the pharmaceutical, biotechnology, and medical device industries.

Validation Professionals, Inc. is seeking a QA Specialist with at least 5 years of Quality Assurance experience in pharmaceutical, biotechnology, or related industry. Responsibilities include batch record/SOP/validation document review as well as support of Quality Systems.

Candidate must have demonstrated competence in cGMP, validation principles, quality expectations, and industry practices.

Candidate must have excellent organizational, oral, and written communication skills. Good interpersonal skills and problem solving skills are required.

BS degree or equivalent in Engineering, Chemistry, Life Sciences, or other job related discipline is required.

Project Manager - Frontier Science/ECOG (Boston)

2009-12-08T11:22:54-05:00

One of the largest clinical cancer research organizations in the U.S., ECOG designs, monitors and manages clinical trials aimed at finding new and better ways to prevent, diagnose and treat cancers in adults. Funded in large part by the National Cancer Institute (NCI), we work with 6000-7000 physicians, nurses, pharmacists, statisticians, and clinical research associates (CRAs) from the U.S. and internationally. Currently, ECOG has more than 90 active clinical trials in all types of adult cancers. Our studies treat more than 6,000 patients per year, many for whom standard therapies have not been effective and few other options remain available.

The Project Manager (PM) is responsible for the oversight and management of a specific clinical trial with a pharmaceutical sponsor. The PM works closely with the Data Management Department Manager, the Industry Manager and the Study Chair to monitor the status of the study. The PM is also responsible for the supervision and oversight of a team of data associates. A successful PM will manage multiple data management priorities and help their staff organize workloads to meet deadlines. The PM must be comfortable working with metric-driven goals. The PM will be familiar with the planned statistical analyses for the protocol, and collaborate with others to develop trial specific SOPs, training material and documentation necessary to provide structure and consistency to the team. This position requires the ability to take initiative and work independently on tasks/ projects, with appropriate judgment and discretion about when to consult the Project Coordinator. The PM will be expected to maintain the utmost knowledge and mastery of the protocol. Travel to bi-annual ECOG Group Meetings may be required

This position requires the following skills and experience:
- Bachelor�s degree or equivalent work and/or life experience
- Minimal of three years experience in clinical trials (oncology a plus)
- Proficiency in of Clinical Data Management procedures
- Knowledge of Good Clinical Practices (GCP)
- Strong computer skills
- Excellent written and verbal communication skills
- Ability to prioritize tasks and work under pressure
- Strong organizational skills and attention to detail
- Familiarity with relational databases and data management software packages
- Demonstrated personnel management skills

All applicants MUST have experience in or demonstrated knowledge of the process of clinical trials. All candidates must demonstrate an ability to manage multiple priorities, an ability to communicate effectively and professionally, and an ability to work under pressure and meet deadlines. This is a full time, 40 hour position, Monday � Friday during normal business hours (8-4 or 9-5).

About Us:
ECOG (www.ecog.org) is one of the largest clinical cancer research organizations in the United States, and conducts clinical trials in all types of adult cancers. We work toward the common goal of controlling, effectively treating, and, ultimately, curing cancer.

Frontier Science (www.fstrf.org), the grantee, is a non-profit foundation and offers excellent working conditions and outstanding benefits, including 4 weeks paid vacation.

Our office is located close to several public transportation routes, including the Green Line B train, the route 57 bus from Allston and Watertown, and the CT2 cross-town bus route between Cambridge and Ruggles station.

How to Apply:
Please submit cover letter with job code PMCL included and resume to resumes@jimmy.harvard.edu. Resumes submitted without a cover letter will not be considered. Please included preferred salary.

EOE/AA

Forms Development Project Coordinator - Frontier Science/ECOG (Boston)

2009-12-08T10:00:48-05:00

Due to new, exciting developments in cancer research, the Eastern Cooperative Oncology Group (ECOG) currently has an opening for motivated, organized, and detail-oriented professionals. The following position requires excellent organizational, interpersonal, and communication skills; the ability to prioritize tasks, meet tight deadlines, work both independently and on a team; database and word processing experience is helpful. BA/BS is preferred; equivalent work and/or life experience will be considered.

The Forms Project Coordinator (PC) is responsible for the oversight and management of the clinical Case Report Forms (CRF) Development process for the department. This process requires close communication with several departments in order to design and implement forms (CRFs) that capture all of the necessary data needed to later analyze the results of the clinical trial. This person regularly conducts quality control reviews of protocols and forms. The Forms PC is a line manager for junior staff involved in the forms development process, and is responsible for all day-to-day activities within the department. The Forms PC is responsible for monitoring the progress of protocols in development to ensure CRF development occurs in conjunction with protocols to ensure timely activation. Additional duties include participation in training programs, and training of staff in the Data Management and Protocol Development departments, as well as Statisticians. The Forms PC works with the Data Management Manager to ensure CRF development and revisions are being done in line with current Data Management data quality controlling policies. This position also acts as liaison with other departments to ensure their needs for the data collected on CRF�s are met. The Forms PC participates in recruitment and hiring, provides direct supervision to the Forms team members, and creates needed documentation such as SOPs, Work Instructions, and educational trainings. The Forms Development PC will participate and take an active role in numerous meetings and conference calls. Required skills and experience include
strong written and verbal communication skills, management experience, experience with clinical trials and demonstrated leadership skills.

ECOG (www.ecog.org) is one of the largest clinical cancer research organizations in the United States, and conducts clinical trials in all types of adult cancers. ECOG�s network includes nearly 6000 physicians, nurses, pharmacists, statisticians, and clinical research associates (CRAs) from the U.S., Canada, and several other countries worldwide. We work toward the common goal of controlling, effectively treating, and, ultimately, curing cancer.

Frontier Science (www.fstrf.org), the grantee, is a non-profit foundation and offers excellent working conditions and outstanding benefits, including 4 weeks paid vacation; paid sick time, paid holidays and personal days. Frontier Science also offers health and dental insurance, 2 retirement plans, fitness reimbursement and tuition reimbursement. Our office is located close to several public transportation routes, including the Green Line B train, the route 57 bus from Allston and Watertown, and the CT2 cross-town bus route between Cambridge and Ruggles station.

Please submit cover letter including salary requirement and job code (FPCCL) and resume to resumes@jimmy.harvard.edu. Resumes submitted without a cover letter will not be considered.

ECOG/Frontier Science is an AA/EOE/D/V

Looking for a Challenge? Try a Sleep Study! (Boston)

2009-12-08T09:01:34-05:00

Participants needed for 9 Day Sleep Research Study on the effects of light on sleep at Brigham and Women's Hospital
Do you fit these qualifications?

*Must be 18-30 years old

*Not on any medications

*Non-smoker

*Sleep about 8 hours/night

THEN YOU MAY BE ELIGIBLE TO LIVE IN A LAB 24/7 FOR 9DAYS/NIGHTS!

Receive up to $1,960

** 3-5 week screening process, up to 5 outpatient visits before entering the study **

Contact Us at (617) 732-4311

Environmental Professional (Concord)

2009-12-07T21:28:15-05:00

Environmental consulting firm is seeking individual with experience in performing Phase I Environmental Site Assessments. Work is project based and very flexible, can be done on a part-time basis.

Please send resume

Research Associate (Needham)

2009-12-07T18:08:05-05:00

Outside The Classroom is the pioneer and leading provider of substance use prevention programs and strategic services for institutions of higher education. Founded in 2000 and based outside Boston, Outside The Classroom has developed a suite of evidence-based prevention programs, online education tools and support services to address the most pressing public health issues facing our nation�s youth.

As a member of the Research and Analysis team, the Research Associate will work closely with the Director of Research to launch new research projects by organizing and cleaning data, running exploratory data analysis, and performing literature review on a variety of topics. This role provides the unique opportunity to be part of small team of behavioral researchers investigating the most pertinent topics relating to substance use and mental health. The current opening is structured as an in-office, full-time position for the first 3 months, moving to part-time for 6 additional months, with the potential for extension beyond that.

Responsibilities (include but are not limited to):
� Assume ownership of a significant portion of the data set-up effort, by retrieving, merging, and cleaning large datasets.
� Play a leading role in conducting exploratory data analysis.
� Support executives and managers in a consultative way throughout ongoing investigations.
� Perform detailed literature review and write up for current projects.
� Communicate effectively with senior management regarding research methodology.
� Help the team by providing unique insights on the data, and evaluate trends as well as emerging themes in data.

Technical Skills & Qualifications:
� Undergraduate degree required; possessing or currently pursuing an advanced degree in psychology, public health, epidemiology, or behavioral statistics preferred.
� Proficiency in using SPSS and SPSS Syntax, conducting data cleaning, and exploratory data analysis on large 100,000 + samples; capable of querying and analyzing complex quantitative and qualitative data sets.
� Proficiency with introductory statistics, as well as some experience with multivariate, multi-level, and forecasting models (e.g. HLM, SEM, ARIMA).
� Some working experience with HLM, AMOS, PASW Forecasting is desired.
� Demonstrated skills using Microsoft Office Suite (Excel/ Word/ PowerPoint).
� Outstanding literature review and writing skills; ability to clearly synthesize, discuss and write about complex concepts in the research literature.

Non-technical Skills & Qualifications:
� Strong analytical thinker, capable of breaking down and working with broad research hypotheses.
� Well-developed problem-solving ability and critical thinking skills.
� Comfort engaging with senior-level administrators.
� Strong interpersonal communication skills.
� Ability to work independently, but also as a member of a team.
� Desire to collaborate with other departments to gather and document requirements and to learn all aspects of program functionality.

If interested please send a cover letter and your CV clearly outlining how your skills and experience meet the requirements of this position. You should also include a writing sample demonstrating literature review, writing and research abilities. Please no phone calls.

Senior Program Director (Burlington, MA)

2009-12-07T16:18:00-05:00

Senior Program Director� Job # 28017
EBI Consulting is a rapidly growing, profitable company, headquartered in Burlington, MA. Our employees are the key to maintaining our competitive edge. To attract and retain the best industry talent EBI shares its success with its employees, and is committed to providing a professional work environment where career learning, growth and recognition are highly valued. If you are seeking an opportunity to work in a progressive organization that will offer you diversified challenges and an excellent opportunity for advancement please review our current employment opportunities. For more information about EBI and open positions please visit our website at www.ebiconsulting.com.

Position Description:
Candidates should have 8-20 years of experience with environmental health and safety issues. Experience in an environmental consulting firm and/or experience as an industrial facility EHS Manager is desirable.

Responsibilities will include:
� Managing consulting projects for industrial and institutional clients.
� Assistance in developing business including outreach sales, development of marketing programs, and sales support.
� Technical and regulatory support to project managers on a wide range of EHS issues.

Education Requirements
B.S. or M.S. in related field

Specify registration requirements.
P.E., CSP or CIH a plus but not required.

Benefits
EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities.
EOE M/W/D/V

Submittal
Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com. You must include the following information:

1. Reference job #, job title and resource
2. Brief summary of past related experience (highlight your experience as it relates to our need & industry);
3. List of your education credentials and professional registrations
4. Salary history

We look forward to hearing from you!

Research Technician (Boston, MA)

2009-12-07T14:55:27-05:00

A technician position is available to study human and mouse models of leukemia using the latest genomic analysis techniques, and to help develop pediatric cancer sample repositories. The research focus is identification of pathways important for leukemia development that can be targeted therapeutically. Projects will incorporate the latest technologies in genomic analysis to study how normal blood cell development is disrupted during leukemia development. A background in genetics, molecular biology, or immunology and previous technical experience is preferred but not required. Experience with mouse model research would be beneficial. Send CV and names of three references to email address above.

Research Associate, Molecular Biology, RT-PCR (South Shore)

2009-12-07T13:11:27-05:00

Research Associate, Molecular Biology, RT-PCR- South Shore, MA

This is a full time position where you will be responsible for supporting Molecular Diagnostic assay development, and Research & Development activities. This is a key position leading the successful development of innovative Molecular Diagnostic products utilizing RT-PCR and Capillary Electrophoresis quantitative detection methods. Your scientific activities will involve:

* Contributing to research and development of molecular diagnostic projects including the execution of clinical study plans, regulatory filings, and interfacing with production, manufacturing, & marketing departments.
* Performing assay development and quantitiative methods for the detection of nucleic acids utilizing PCR, RT-PCR (Real-Time PCR), Capillary Electrophoresis, and nucleic acid chemistry.
* Leading verification studies and validation for the development of molecular diagnostic products.
* Contributing to FDA regulatory filings and 510(k) submissions for CE marked products.
* Maintaining, troubleshooting and optimizing laboratory production equipment.

Preferred Candidate Background and Expertise:

* BS degree in Biology, Chemistry, Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering or related Scientific/Engineering field.
* 1-3 years of industry experience involving Molecular Biology related R&D.
* Hands-on scientific expertise performing PCR, RT-PCR, Cloning, Sequencing, nucleic acid extraction, Capillary Electrophoresis, oligo synthesis, nucleic acid chemistry, or enzyme chemistry.
* Expertise working within ISO, CE Marked, & FDA compliance and providing required documentation.

PLEASE APPLY FOR IMMEDIATE CONSIDERATION: http://www.resuwe.com/jobDescription.jsp?jobId=185

Lab technician/Junior scientist - Work with lab mice & rats (Lawrence, MA)

2009-12-07T12:06:02-05:00

Hooke Laboratories, Inc. is a small biotechnology service and product company.

Our web page is http://hookelabs.com

We have an immediate opening for an entry-level lab technician/junior-level scientist.

This position is for laboratory work in experimental biology and medicine. You'll be
working with laboratory mice and rats - caring for them, monitoring their health,
administering drugs, etc.

You must be flexible re work hours; this position includes some evening and weekend
work (usually one day per weekend).

The ideal candidate will have a degree in biology, the physical sciences, medicine,
or engineering.

You must be:

* Willing to handle animals
* Flexible
* Ready to learn and work hard at doing good science for our customers

We will also consider part-time positions for college students.

All positions are at our facility in Lawrence, Massachusetts, close to I-495.

Please send your resume or CV via email. Include your GPA.

Hooke Laboratories is an Equal Opportunity Employer.

Product Manager New Product-0901388 (Rockland, MA)

2009-12-07T10:19:14-05:00

At EMD Serono, Inc. our strength is our people!

About the Company

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.

Description

In this role you will make a significant contribution to the Consumer Marketing Team for a product that has the potential to meet a significant unmet need for people living with MS. During the pre-launch period ensure the tactical plan is implemented effectively so the appropriate promotional and educational materials are prepared for drug approval. as well as contribute to the development of promotional materials and consumer programs / initiatives based on clinical data and other key selling points relevant to patients.

KEY TASKS & RESPONSIBILITIES

Think with a "patients first" attitude in the development and execution of marketing tools, programs, and services that fulfill strategies which include, but are not limited to live patient programs, development of patient educational content & tools via the web and traditional modalities, patient ambassador development and patient tools/kits
Own and execute specific initiatives within the consumer tactical plans for the brand
Ensure consumer messaging is built into all promotional activities
Work closely with Senior Product Manager to implement highly interactive patient Consumer Relationship Management program
Use social media and web assets to increase patient awareness and relationships
Iterate and refine initiatives and programs taking into consideration the changing competitive landscape including other emerging therapies, new clinical data, and emerging market research findings. Work with the Senior Product Manager of Consumer Marketing to ensure that these initiatives fit with the overall strategy.
Work with legal, regulatory and medical committee to ensure approval of assigned marketing collateral
Work in close collaboration with business intelligence and market research on the development of research tools and analysis of results to better refine consumer programming and initiatives.
Work in close collaboration with field sales management and patient service center to ensure successful development and implementation of programs, tools, and services
Work with Marketing Advisory team to develop and adapt plans, support implementation of new and unique customer programs, and value-added services, etc.
Conduct field visits as necessary to evaluate effectiveness of marketing programs, tools and services.

Qualifications

EDUCATION & LANGUAGES

BA/BS required
MBA or advanced degree preferred

PROFESSIONAL SKILLS & EXPERIENCE

A minimum of three years related marketing experience in pharmaceutical/biotech industry
Expertise in digital media, web for patient audience
Experience in developing patient educational programming preferred
Strong pharmaceutical marketing experience with consumer audience preferred
Familiarity and experience with patient ambassador programs preferred
Experience with Customer Relationship Management Programs
Experience working with vendors and contractors,li>Previous pharmaceutical sales or market research experience a plus

PERSONAL SKILLS & COMPETENCIES

Strong communication skills and an ability to translate medical information into succinct and high impact marketing messages for consumer audience
Understanding of patient educational needs
Ability to work in fast paced environment
Ability to analyze competitive landscape and key brand issues and ascertain best use of brand budget on consumer audience
Must be comfortable with ambiguity common in pre-launch environment
Have the ability to multi-task and have superior organizational skills
Excellent interpersonal skills
Ability to access and influence various functional areas and motivate groups to actions through team building initiatives
Leadership skills in a matrix, and/or co-promote environment,li>Collaborative work style and familiarity with core operating function (sales, marketing, regulatory, legal, medical, global marketing and co-promotion partners)
Business oriented thinking
Strong PowerPoint and excel knowledge
Strong Presentation skills
Relationship Management Skills
Position requires both domestic and international travel up to 30-40% of time. Some domestic travel peak times in the first few months of this role may be up to 60%.

Click the link below and open the door to the future by submitting your resume today!

EMD Serono 0901388

Awards & Recognition

June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!

May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

TIME FOR A CAT NAP? (Boston, MA)

2009-12-07T09:03:12-05:00

People 18 and older with no sleeping problems!

Brigham and Women�s Hospital
is conducting a research study on
the effects of LIGHT on wake and sleep

Complete up to five screening visits
then live in a lab for 3 days
Receive up to
$850

Interested? Contact Us!
Department of Medicine
(617) 525-8904

Product Manager (Proteomics) (Boston)

2009-12-07T08:38:46-05:00

This is an excellent marketing opportunity for anyone who is able to travel 2 weeks a month.

This is a strategic and tactical Product Manager Position. Candidate must be savvy in both reagents and capital equipment, however more focus is on the instrumentation.

Key Words: Molecular biology, image analysis, DNA, genomics, genetics, proteomics. reagents, OEM, software

We are looking for a real team player with the highest integrity; someone who is looking for a career/ long term position.

We prefer at least 4-5 years of industry specific experience in addition to an MBA. We can only consider candidates who have biotech/biopharm experience.

Company is top notch with excellent benefits.

Thanks for your time and interest. Please send resume in word doc attachments.

RESEARCH POSITIONS AT MGH:Analysis of Cancer & Math/ComputerAps In Med (Cambridge)

2009-12-07T00:03:06-05:00

Several full time research positions are available at the Massachusetts General Hospital for graduating seniors interested in spending a year or two before continuing their education in medical or graduate school, as well as for individuals with somewhat more experience, including students with Masters Degrees. Previous holders of this type of position have had the opportunity to work on research projects and to publish scientific papers on their work, and many individuals have published first-authored papers on their work. For students with an interest in medicine, exposure to clinical medicine is encouraged. The work of our group has concerned: the assembly of data, and the development of improved mathematical methods, for predicting the outcome for cancer patients; the identification of screening schedules for reaching the maximal possible reduction in cancer death achievable by cancer screening; the application of modern computer speech and telephony for developing scheduling/reminder systems for increasing the use of preventative medical interventions such as mammography and influenza immunization. The program is a collaborative project between individuals at the Massachusetts General Hospital, Harvard, and MIT, and is located in an MGH facility next to MIT in Cambridge.

These positions are available as of June 1. But students who wish to begin working part time in the spring semester are encouraged to do so.

The first position concerns the assembly and analysis of data on cancer and its outcome. An interest in medicine, and a familiarity with the use of Excel and Access is essential. The candidate need not have a strong background in mathematics or computer science, although this would be desirable.

The second position concerns the analysis of the systems that hospitals use to make medical appointments, with the aim of improving utilization of preventive service such as cancer screening.

The third position concerns the refinement, implementation, and testing of a system that sends computer generated telephone reminder messages for increasing the use of breast cancer screening. Knowledge of, or ability to learn, ASP, ASP.net, AJAX, C#, HTML, MS SQL Server, Windows Server 2003 security, and general database and server administration is required. Skill with VXML and computer speech would also be desirable.

The fourth position concerns the development of improved mathematical methods for predicting cancer outcome. Related work concerns the development and implementation of novel mathematical methods for Web-based calculators that physicians can use for predicting the risk of cancer recurrence, as well as the development of computer simulation models of cancer progression.

The fifth position concerns the creation of telephone reminder scripts, which our systems will launch to recruit patients to schedule appointments for cancer screening. This position would be suitable for a person with interests in advertising, copywriting, English, marketing, social marketing, persuasion psychology, health communication and public health.

Reply by email with CV or resume to:

James S. Michaelson Ph.D.
Department of Pathology
Harvard Medical School
&
Departments of Pathology and Surgery
Massachusetts General Hospital

Technical Assistant I - Lodish Lab (Cambridge, MA)

2009-12-04T15:06:02-05:00

OVERALL RESPONSIBILITY

Designs and performs bench level experiments and small independent research projects to support scientific research aimed at identifying genes that regulate metalloprotease cleavage of substrates like EGF ligands, with the goal of developing new therapies for cancer, heart disease and kidney disease. Analyzes experimental data, addresses methodological problems in experimental protocols and results, and reports data to supervisor. Uses discretion in prioritizing and organizing workflow and in optimizing methodologies and results.

CHARACTERISTIC DUTIES

� Major Responsibilities include: standard molecular biology assays, cell culture, flow cytometry
� In consultation with the Principal Investigator or other project manager, designs and conducts bench level experiments and small independent research projects.
� Independently operates lab equipment and prepares, orders, and maintains stocks of necessary reagents, solutions and supplies. May work with vendors to address equipment, reagent, or supply issues.
� Performs analysis of experimental results by identifying methodological problems and helping to identify and implement modifications in research protocols.
� Documents, compiles and assists in interpreting experimental data. Reports data to supervisor in oral and written reports.
� May assist Technical Associate or project manager with determining the order of research processes that best support essential project goals.
� Operate and maintain laboratory equipment to complete investigations.
� May consult scientific literature as needed.
� Other tasks as required or assigned.

QUALIFICATIONS

� Bachelor�s degree in Biology or related field
� 1 year of experience working in a research laboratory preferred.
� Proficiency in basic lab techniques and principles of molecular biology required.
� Knowledge of various scientific databases required.
� Excellent written and oral communication skills, strong organizational skills required.

Interested candidates should send resume to:
Rodney Byrd
The Whitehead Institute for Biomedical Research
9 Cambridge Center
Cambridge, MA 02142
resumes@wi.mit.edu