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They will partner with Commercial, Research and Development, Clinical Development, HEOR, and Regulatory Affairs. This role will report to the VP, Medical Affairs and will lead medical activities through the successful execution of the oncology medical affairs strategy and tactical plan.
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You will be a strategic partner to comms leadership, gathering qualitative and quantitative insights on the most business-critical priorities - across product, public affairs, tech policy and business strategy.
$242,000 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Your choice of a career at the U.S. Department of Veterans Affairs (VA) means joining thousands of physicians, nurses, mental health and allied health professionals, pharmacists and nonclinical support staff building careers based on giving back.
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Title: Vice President of Quality Assurance & Regulatory Affairs. Proficient with the design, implementation and maintenance of quality management systems for medical device development, manufacturing, distribution, and post market surveillance.
$325,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum of 3-5 years of experience in medical affairs or a related field. Jasper is a clinical-stage biotechnology company developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases such as chronic urticaria and lower to intermediate risk myelodysplastic syndromes (MDS) and as a conditioning agent for stem cell transplants for rare diseases such as sickle cell disease (SCD), Fanconi anemia (FA) and severe combined immunodeficiency (SCID.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Resident Director Vice Provost for Student Affairs, Stanford, California, United States Student Services May 09, 2024 Post Date 103190 Requisition #Residential Education facilitates an undergraduate residential experience in the neighborhood setting that fosters diversity, equity and inclusion, health and well-being, belonging and community, and intellectual and personal growth.
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Description: Regulatory Affairs CMC – Data Administrator Contractor. Work is performed under the general supervision of more senior Regulatory Affairs CMC Systems professionals. Description: Regulatory Affairs CMC – Data Administrator Contractor.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Sr. Manager is responsible for providing strategic direction, operational support, and technical expertise for CMC regulatory activities and related regulatory initiatives.
$96 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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In this role, you will be responsible for generating competitive intelligence; supporting our market strategy, sales and public affairs teams, and providing technical expertise during customer, partner, and regulatory interactions.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
$113 an hourFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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You have familiarity with the real world data and evidence space, have worked in the rare disease space, and have sold into both early stage biotechs and big pharma across R&D, clinical development, medical affairs and post-marketing teams.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Collaborate with other applicable functional area specialists including with Clinical Research, Regulatory Affairs, Biostatistics and Data Management, Translational Medicine, Contract Research Organizations (CROs), Data Monitoring Committees (DMCs), business partners and other entities, as needed, to evaluate and manage safety signals for ZW products; provide support to cross-functional ad-hoc teams set up to address urgent and important safety issues.
$178,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees and other support for Scientific Communications. Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Preferred experience in Medical Affairs and/or Clinical Research including Phase IIIb and IV studies; clinical trials management, medical monitoring and scientific expertise. This contractor role is within the LIFE (Liver, Inflammation, Fibrosis and Established Products) Medical Affairs organization and reports to the Executive Director of Global Medical Affairs, Hepatitis C.
$55.98 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago
affairs job in Redwood City, CA
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