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Under the guidance of the Director of Dive Programs, helps develop field scientific diver training. Preferred active Scientific Diver certification as defined by the American Academy of Underwater Sciences.
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Employer: Celgene CorporationPosition: Scientific Associate Director (ref. Act as a technology expert and scientific liaison for several external research partnerships of high strategic importance to BMS. Lead the biology team for one of BMS' small molecule drug discovery programs.
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Offer scientific, strategic, and practical guidance across the entire spectrum of pharmaceutical drug product development, covering pre-formulation, formulation development, non-clinical and clinical manufacturing, and preparations for commercialization.
$220,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate with research scientists and data analysts to identify computational needs, translate scientific questions into analytical workflows, and provide guidance for data processing, quality control, and statistical analysis.
$200,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Scientific Director will serve within the Oncology Translational Research. Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for a Senior Director-Oncology Translational Research - Multiple Myeloma, located in Spring House, PA; Boston, MA; Raritan, NJ; Brisbane, CA or Remote (considered on a case-by-case basis.
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Supporting Pfizer Oncology, you will be a senior scientific and strategic leader and a member of the Pharmacometrics and Systems Pharmacology Leadership Team. In this key role, you will influence the discovery and development of drugs and expand the application of model-informed drug development (MIDD) approaches within oncology and across our portfolio.
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The Director, Product Management will report to the VP, Product Marketing and oversee PacBio’s short read product marketing efforts by leading the product marketing function to develop and deliver a fully integrated marketing strategy for the business – across product, promotion, pricing and sales enablement.
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Sales experience in the test and measurement industry preferred; other relevant experience will also be considered, e.g. technical sales, selling hardware / scientific instrumentation to industrial, academic, and research customers.
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Partner with your District Sales Manager and Regional Sales Director to develop a local strategy and business plan to generate recognizable increases of sales in your territory. As a Pharmaceutical Sales Specialist for R&I Primary Care Team, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives.
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Extensive knowledge of clinical drug development is mandatory and should include prior experience with clinical development planning, regulatory requirements and documents, study design, biostatistics, monitoring, data handling, data analysis, report writing, and scientific presentation of data.
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The Associate Director of Regulatory Affairs (RA) Labeling will assist in the development of a cross-functional labeling strategy for products worldwide, including providing expert input on labeling requirements and strategic guidance during label development, facilitating cross functional labeling discussions with Labeling Management Team (LMT) and Executive Labeling Committee (ELC) as appropriate, and participating in label-related Health Authority negotiations.
$185,000 - $230,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Requirements Education & Experience: BS in related scientific discipline, and 10+ years of experience in regulatory affairs. Knowledge and Competencies: A scientific and clinical understanding of the regulatory sciences.
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Expertise in medical and scientific fields is crucial for the success of clinical trials and development of effective treatments. Provide clinical and scientific input for study design, protocol concepts, statistical analysis plans, and reporting to ensure valuable clinical endpoint insight for future decision-making.
$300,000 - $360,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our revolutionary Nanoimager stands at the forefront of advancing cellular studies on a molecular level, making substantial contributions to the evolution of scientific knowledge. At ONI, we are driven by a profound mission: to propel scientific discovery and combat diseases by granting everyone the ability to visualize, comprehend, and share the intricate microscopic details of life.
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Arrowhead is seeking an experienced Regulatory/Medical Writer to lead its Medical Writing Team. The Regulatory/Medical Writer will work collaboratively with Arrowhead's regulatory, clinical and scientific teams to produce high quality documents to support the company's drug development programs.
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scientific director jobs in San Diego, CA
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