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Serve as USMA Head of HIV Treatment in cross-functional meetings, representing the US perspective and needs in working groups with Clinical Development, Global Medical Affairs, US Commercial, US Government Affairs and Policy, US Public Affairs, US Regulatory, and US legal and compliance.
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We are seeking a detail-oriented Data Administrator Contractor to support the Regulatory Affairs CMC team. Work under the supervision of senior Regulatory Affairs CMC Systems professionals.
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Represent Global Regulatory Affairs on the Global Artwork Team; help develop, review, and approve global package artwork in close collaboration with Supply Chain, Quality Assurance, and International Regulatory Affairs colleagues.
Part-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This position will report directly to the VP, Regulatory Affairs and will collaborate across the organization to implement and maintain a standardized document development process for regulatory documents.
$213,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The incumbent will report directly to Head of CMC Regulatory Affairs – Systems and Operations at Gilead. In addition, the Sr Director will be accountable for leading the interpretation and implementation of new and existing CMC regulatory guidelines and regulations to ensure approvability globally.
$307,560Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Vice President of Medical Affairs is responsible for providing clinical and scientific guidance in all areas of clinical risk, safety reviews, adverse experience reporting, product life cycle reviews, and protocol design.
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HEALTH- Guardant Health, Inc. in Palo Alto, CA seeks Regulatory Affairs Specialist: Examine, evaluate & investigate eligibility for or conformity with laws & regulations & perform other compliance & enforcement inspection & analysis activities.
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Write and edit clinical and scientific reports for regulatory submission and scientific communication. Leverage internal and external resources to establish core domain expertise for medical affairs and clinical affairs initiatives.
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The Decedent Affairs Coordinator will interact with physicians, nursing staff, Pathology Department, police, medical examiner, risk management, security, etc. The Decedent Affairs Coordinator is responsible for coordinating the care of deceased patients after a demise within Stanford Health Care and Stanford Children's Health.
$39.28 - $51.07 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our client is currently seeking a Regulatory Affairs for a 12 month + contract. Knowledge of regulatory guidance documents (FDA, Health Canada, EU MDR) for determining if a product change requires a regulatory submission (software and hardware devices.
$50 - $68 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Email res (must reference Job Code #43428) to resumes@guard anthealth.com. Part-time telecommut-ing allowed.
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The Director of Regulatory Affairs will support product development, registration, and post market support activities, in addition to managing a small team of Regulatory Affairs Associates and directing their work as it relates to the activities outlined below.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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They are looking for a Senior Director of Regulatory Affairs, Ad/Promo to join their team to support the commercialization of their late-stage programs. Senior Director, Regulatory Affairs - Advertising and Promotion.
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BA/BS or advanced degree in life sciences or related field with some related work experience in the biopharma industry, e.g., clinical R&D, regulatory affairs, quality, or other related discipline.
$149,160 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Executive Director of Regulatory Affairs will lead the Regulatory Strategy group and be accountable for the delivery of regulatory strategy at RevMed. They will support regulatory strategy program leads and ensure delivery of targeted, pragmatic, well-vetted, consistent, and actionable regulatory advice across oncology drug development programs.
$305,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
Title: regulatory affairs Company: Parexel in Redwood City, CA
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