R & D Jobs in Medford, Massachusetts

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290 Medford, MA R & D jobs found on Monster.

Jobs 1 to 20 of 290
. We are currently looking for a QC/QA Analyst with strong background with Biomedical/Pharma companies. This is a 8month+ contract in Medford, MA please email your resume to ***** for review. Job Summary Responsible for mechanical, chemical, and microbiological testing in support of Manufacturing Operations raw material, in-process and product release samples. Responsible for...
CROMSOURCE is an international, full-service Contract Research Organization resulting from the acquisition of MSOURCE by CROM Group. For more than 20 years we have provided ISO certified clinical development services to the pharmaceutical, biotechnology, vaccine and medical device industries for products and devices in a broad range of therapeutic areas. To ensure the success of our clients, our t...
CROMSOURCE is an international, full-service Contract Research Organization resulting from the acquisition of MSOURCE by CROM Group. For more than 20 years we have provided ISO certified clinical development services to the pharmaceutical, biotechnology, vaccine and medical device industries for products and devices in a broad range of therapeutic areas. To ensure the success of our clients, our t...
STI-ECD-512-(B) Crystal16 PROCESS CHEMIST SCIENTIST- Easymax, HPLC- Arlington, MA Location: Arlington, MA Domain: Research Job Type: Direct Job Description: In this role the scientist will be responsible for developing scalable, cost-effective, and manufacturing friendly down-stream process (DSP) methods to produce quality APIs for advanced biological evaluation. The successful candidate will effi...
WHEN WE RECEIVE YOUR RESUME, WE WILL SEND YOU A COURSE ON HOW TO BECOME AN INTERVIEW SUPERSTAR. IT IS FREE BUT IF WE CHARGED THOUSANDS IT WOULD BE WORTH IT. ASSOC DIR BIOSURGERY REGULATORY AFFAIRS (RK) Pharmaceutical / Biotech Root of Jobs - Research & Development Full-time United States - Massachusetts - Cambridge Jobs ID - 916864 The Compensation Benefits - Full Relocation Assistance Available -...
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Statistical Programmer 2 Why Quintiles? • Largest CRO in the world with over 27,000 employees globally. • Ranked 6th in InformationWeek 500 Computerworld Magazine’s “100 Best Places to Work in IT" • Ranked 25th in the inaugural World’s Best Multinational Workplaces list from the Great Place to Work Institute. • Outcome is the late phase and observational study division of Quintiles. We doubled in...
This Senior Clinical Operations Specialist is responsible for managing the oversight and implementation of biomarker strategic objectives. Responsibilities include budget and contract management, sample quality, timeliness and biomarker administrative needs (budget, presentations and study documents). This role is responsible for all budget and contract management related to biomarker related rese...
Job Description: Responsible for ex-US Clinical Trial Application (CTA) submissions to national competent authorities (to include initial submissions, amendments, notifications and report), the level of support to vary depending on whether a CRO or affiliate is performing the submission. Analysis of regulatory issues and guidelines related to clinical trials. Responsible for accuracy and content o...
HOT new Cambridge Start-Up seeking Director, Purification Biologics to join their growing and dynamic team! This role will be responsible for building and leading the purification and process development team that will drive their research and development strategy. Specifically responsible for the following but not limited to: · Develop robust and scalable purification process capabilities to info...
PURPOSE Engage in company training program to gain knowledge and skills required to independently contact investigative sites and participate in clinical research. Collect, compile, document and support clinical research data via remote site monitoring. May be responsible for the remote monitoring of multiple projects. RESPONSIBILITIES Complete appropriate therapeutic, protocol and clinical resear...
Quintiles, the world's largest CRO has had great success in winning new contracts. Become involved in work that improves the quality of life for people around the globe. Let your career soar with an established and successful company where an individual can make a difference. We are seeking a motivated Senior Project Coordinator. The Senior Project Coordinator will support and coordinate project a...
We are looking for a highly motivated individual to be a key contributor in the Sample Management Group (SMG)). As a member of the Sample Management Group, the successful candidate will be primarily responsible for plate production to support high and medium throughput screening efforts. Key Functions: Primary responsibility will be the storage, retrieval, replication and distribution of proprieta...
We have a Contract opportunity with a prominent client for a Senior Associate II, Regulatory Affairs in Cambridge, MA. Description: *Must possess exceptional communication skills (both written and verbal) *Will be required to communicate with all levels within the organization Job Title: Senior Associate II, Regulatory Affairs Responsible for ex-US Clinical Trial Application (CTA) submissions to n...
R&D Information Services Bioinformatics Programmer – 4 month contract We seek a bioinformatics programmer to join a dynamic Next Generation Sequencing (NGS) analysis core group supporting translational medicine, discovery and development groups across Sanofi. As an integrated part of the core group, the contractor will: Develop and maintain automated analysis and quality control pipelines for a va...
Production Control Planner/Scheduler Location: Cambridge MA Position Summary Gen9’s manufacturing organization is seeking a customer-focused Production Control Planner/Scheduler to ensure our operations run effectively and efficiently. Reporting to the Director of Manufacturing, the Production Controller will prioritize the day-to-day production as well as participate in scaling and improvement ac...
Scientist I – 9 month contract We are seeking to fill a contract position in Biochemistry and Bioanalytics group to contribute to the early stage oncology drug discovery research in Sanofi. The successful candidate will involve the biological sample preparation and consequential analysis of molecules ranging from small molecule to proteome with advanced mass spectrometers to identify clinically tr...
Associate Research Scientist III – 6 month contract with a 1 year extension Hands-on responsibilities will include assisting in the development of new vaccine delivery systems, assay development and supply of formulations for in vitro/vivo testing. Requirements BS in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering or related discipline is required with 0 - 3 years of laboratory re...
Description: A Research Associate (RA) in Optum Labs will work on a variety of health care research projects. The RA will assist researchers and analysts in the conduct of research studies. The RA will also participate in research infrastructure projects, support operational activities and perform administrative tasks. Work is conducted in a collaborative, multi-disciplinary, academic partnership...
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