Natural resource biologist jobs in the Biotech, R&D, Science category

We seek an experienced bioinformatics scientist / computational biologist to work with therapeutics groups across the sanofi families of companies in Boston. As an part of scientific teams identifying both targets and patient selection biomarkers, you will Develop analysis and quality control pipelines for a variety of Next Generation Sequencing (NGS) applications such as DNA-seq, ChIP-seq, and RN...
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Company Overview: Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health. The pharmaceutical industry is a complex, r...
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We are seeking a hands on molecular biologist to perform DNA-RNA manipulation, enzymatic modification of nucleic acid, whole genome amplification, next gen sequencing, DNA isolation, real time PCR, and bioinformatic analysis. Shall: * Develop reagents to prepare clinical specimens for molecular amplification and analysis * Scale up and transfer reagents from development into manufacturing High gro...
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Seeking a molecular biologist to develop, scale up and transfer reagents from development into manufacturing Perform: * DNA isolation from various sources * Enzymatic DNA Modifications * Nucleic Acid Manipulation * Next Gen Sequencing * whole genome amplification * Preparation of libraries for real-time PCR, microarrays, and Next Generation Sequencing Offering competitive salary and benefits, indi...
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Our very well funded, Cambridge, MA based client has science that has the potential to make radical improvements towards human life. If you are seeking to join a company that is very well funded, lead by the very best and brightest, with science stemming from one of the worlds leading labs you have to consider this opportunity. It simply doesn’t get better than this. Sought is a Cell Biologist who...
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TechData is hiring Biostatistician (some can telecommute), SAS Programmer (Some can be telecommute), Sr. Clinical data manager, Sr. Medical Writer,Life Sciences Hub (LSH) Consultant and Oracle Clinical for Global Librarian/Modeler, Biomarker Trial head for our pharmaceutical clients in Northern NJ. Please see below requirements and send your inquiry and resume to: dan.chen@techdataservice.com or r...
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Catalent Pharma Solutions (a Blackstone Group company) is a leading Drug Development, Advanced Delivery Technology and Supply partner to the global pharmaceutical industry. A Fortune 1000 company, with over 20 locations on 5 continents, we partner with 90 out of the top 100 pharmaceutical companies and 44 of the top 50 biotech firms, as well as thousands of small innovator companies. I. Job Summar...
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Research Scientist III, Protein Sciences Reports to: Director of Protein Sciences Location: Cheshire, CT Global Level: 9 Alexion Pharmaceuticals, Inc. is a biopharmaceutical company focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products. Alexion is the global leader in complement inhibitio...
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Johnson & Johnson companies are equal opportunity employers. Head, Computational & Systems Biology-3489120829 Description Janssen Research & Development, L.L.C., a Johnson & Johnson company, is recruiting for a Head, Computational & Systems Biology (CSB) to be located in Spring House, PA. Janssen Research & Development, L.L.C. is a fully integrated biopharmaceutical and biotechnology company. As a...
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Our Client in the South SF area is looking for a Research Associate to join their team! Research Associate Duties: - Participate in efforts to improve properties of engineered enzymes and protein complexes through high throughput screening - Library construction and quality control, protein expression and purification, and assay development and analysis (fluorescent and ELISA-based readouts) - Res...
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ConsignMed, a Niche Clinical Staffing Company since 2003, and rated by Diversity Business as one of the fastest growing companies in the US is seeking a PSUR Safety Medical Writer. The required skill sets/experience includes the following: Candidates must have experience working with Safety reports and must have hands on experience authoring of PSUR reports. Ability to interpret, analyze and clear...
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Primary Role: The Discovery Medicine Director will serve a key role in providing solid clinical expertise to Shire HGT's early Drug Discovery and Translational Research programs in rare and orphan diseases. The primary focus of this role will be in the selection of disease indications and targets based on clinical need and alignment of these research programs through in vitro and in vivo proof-of-...
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FORMA Therapeutics Inc. is seeking to recruit a talented and enthusiastic individual to join a team of scientists supporting compound library management operations in our Branford, CT facility. This position requires a highly motivated individual seeking a unique blend of natural science and technology. This position’s responsibilities will include: compound handling and preparation activities to ...
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Quintiles organization has more depth of therapeutic expertise and a broader range of services than any other service provider. We support both US and Global trials in all therapeutic areas. In fact, Quintiles supports more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! Quintiles is seeking...
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TechData is hiring SAS/Stat Programmers (Some can be telecommuting), Biostatistician (Can telecommute), and Architect in Gaithersburg, MD. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitive pay rate and benefits. TechData is the leading supplier in the pharmaceutical consulting industry. Sr. SAS Pr...
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Title: Senior Clinical Programmer (3 Openings) Reports to: Senior Manager, Clinical Programming Location: Cheshire, CT and Cambridge, MA Position Summary The SeniorClinical Programmer will be a primary resource for the development and validation of programs which create and transfer data across multiple data management systems conforming to Alexion and SDTM standards. Additionally, he/she will be ...
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TechData is looking for Validation Analyst (6 positions), Sr. Drug Safety Associate, Computer System Quality Assurance, SAS Programmer (Some can be telecommuting), Biostatistician, Sr. Clinical Data Manager for our pharmaceutical clients in SFC, CA. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitiv...
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Our customers and their needs continue to evolve. Understanding their touchpoints is essential to improving their experience and our resource allocation. Touchpoint Optimization encompasses the understanding of our customers’ experience in each touchpoint, the processing of the data generated in these touchpoints, and the application of appropriate measurements and analytics to increase the confid...
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Job Title: Clinical Trial Leader Position Description Accountable for all aspects of assigned OTM clinical trials (Phase I/II) including leading Clinical Trial Team(s) (CTT). Number of clinical trials depends on the workload and complexity of the individual trials. Responsible for program level activities as assigned. Position Responsibilities Lead the clinical protocol development process in coll...
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Job Title: Clinical Trial Head Position Description Accountable for all aspects of assigned OTM clinical trials (Phase I/II) including leading Clinical Trial Team(s) (CTT). Number of clinical trials depends on the workload and complexity of the individual trials. Responsible for program level activities as assigned. Position Responsibilities Lead the clinical protocol development process in collab...
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Growing global manufacturer of pharmaceutical API’s needs a Project Manager to work on Methods Development and Validation Projects. Methods validation is one of the most crucial components of pharmaceutical regulatory submission. Projects are designed to evaluate existing or new methods for meeting performance criteria described in the validation protocol. This job is for an analytical chemist, bi...
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Manager Clinical Trials My client is a pharmaceutical company that specializes in treatments that help people with central nervous system disorders and respiratory ailments and has multiple marketed drugs around these therapeutic areas. This company is looking to bring on board a Clinical Trial Manager. This is a key role within the organization, reporting into the Senior Manager/Associate Directo...
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Drug Safety Associate Competitive package Location – North Wales, Pa The successful candidate will process and track Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information. They will also ensure all ICON, Sponsor, and regulatory timeframes are met for the processing and reporting of safety information. Overview of the Role Document a...
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Growing and well-respected biomedical (clinical, basic and applied) research firm has job opportunities at Wright Patterson Air Force Base. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Chief, Research Oversight & Compliance for the Day...
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General Summary: Resource planning (personnel and equipment) resulting in an efficient execution of all projects from sample receipt to report writing, resulting in maximum billability. Timely and properly training of all personnel. Timely and properly maintenance and validation of all equipment. Making sure the Lenexa organization continues to work on harmonizing its processes and systems with th...
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