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Requirements:Advanced degree in life sciences in one or more of the following: MD, DO, PharmD, PhD, and 2+ years of relevant Medical Affairs (medical device/pharmaceutical industry), managed care, and HEOR experience, required.
$191,335 - $247,610ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Director, CMC Regulatory Affairs – Biologics. Head of CMC Regulatory Affairs – Small Molecules. Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams.
$177,905 - $230,230Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a key member of Adicet's medical team, the head of Medical Affairs will be responsible for setting up and overseeing effective interactions with key opinion leaders, patient advocacy groups, and medical institutions in areas of hematology-oncology and autoimmune diseases relevant to Adicet's pipeline.
$297,000 - $409,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Kimley-Horn has an opportunity for a motivated MEP Project Manager/ Senior Design Engineer with a strong healthcare focus (OSHPD/HCAI) to expand our MEP Practice in San Mateo, CA! At least 4+ years of proven experience in MEP design and project management within the civil engineering sector, with a focus on OSHPD/HCAI regulated projects.
$145,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role is expected to closely collaborate with multiple teams across Process Development, MSAT, Analytical Development, Regulatory Affairs, Quality and Manufacturing. Author and review plans, protocols, technical reports and CMC sections of regulatory submissions.
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Senior Regulatory Affairs Specialist, Redwood City, CA - Develop strategies for global approvals to introduce new Spinal cord stimulation systems to market, maintain existing products, provide advice on regulatory requirements, prepare worldwide submissions, and negotiate approval with global regulatory agencies.
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Collaborate with cross-functional teams, including Medical Affairs, Clinical Research, Regulatory Affairs, Biometrics, and Quality Assurance, to provide expert input on safety-related matters throughout the product lifecycle.
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Rudolph & Sletten, a Tutor Perini Company, is seeking a Senior Project Manager to join our office in Menlo Park, CA About Rudolph & Sletten:In the last six decades, Rudolph and Sletten has built thousands of projects across our five California offices, from research centers designed to cure diseases, to institutions that educate future generations, to civic facilities and high-tech campuses that move our state forward.
$180,000 - $215,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We're interested in working with people that have developed and maintained accurate accounts of company affairs and have managed investor reporting requirements. 5+ years of experience in one or more of the following areas: equity research, investment banking, investor relations, or management consulting.
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Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need.
$133,280 - $172,480 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Sodexo is seeking a 3rd Shift Patient Equipment Manager for Stanford Hospital , located in Palo Alto, CA. The Patient Equipment Manager to manage the third-shift, Monday - Friday, 9:00pm to 6:00am.
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As a Finance Manager , you will be responsible for assisting sales consultants and customers with the dealership's financing opportunities and insurance alternatives. Swickard has positioned itself as a leader in highline brands such as Mercedes Benz, Toyota, Lexus, Porsche, Audi, and Jaguar-Land Rover among others.
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Provide to Regulatory Affairs any applicable information or sections of IND/IMPD/CTA/etc. Key interactions are with Clinical Operations, Clinical Development, Pharmaceutical Development, Quality, and Regulatory, and with external vendors (packaging, IRT.
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The Clinical Data Manager / Senior Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team goals and objectives, including oversight of the CRO DM Vendor, if the project is outsourced.
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Clinical Operations plays a key role in ensuring all Client clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Client products.
$86TemporaryExpandApply NowActive JobUpdated Today
affairs job Title: regulatory affairs project manager Company: Gpac in Foster City, CA
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