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Job Title: Senior Manager, CMC Regulatory Affairs, BiologicsDuration: months (we would like to start with months, with the potential to extend if the person is highly competent and a good resource for our team)Location: Remote but preference is to have a candidate available to be onsite at the Foster City, CA offices - days if possible RESPONSIBILITIES MAY INCLUDE.
$90 - $101.35ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Applicants should have a law degree from an accredited law school and a minimum of eight years of relevant experience gained in private practice or as in-house counsel, ideally in the higher education space and with student affairs legal experience.
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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.
$55 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The CMC Regulatory Affairs Sr. Manager at Gilead is responsible for providing strategic direction, operational support, and technical expertise for. Initiates process improvements and contributes to global process improvements, which have a significant impact for the Regulatory Affairs CMC Department or development matrix teams.
$199,320 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Administrative Division Director oversees and manages financial and administrative affairs of the Division of Critical Care Medicine, Pulmonary Medicine, and Quality of Life and Pediatric Palliative Care consistent with standards of performance that ensure University, School, LPCH, and Department business standards and objectives are met.
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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.
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Carry out advocacy strategies to influence policies that impact pediatric rare disease patients and Soleno in collaboration with government affairs consultants. Minimum of 5-7 years of experience in government affairs, lobbying, or a related role, with a strong understanding of the legislative and regulatory process.
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Senior Regulatory Affairs Manager (Open to Remote, Hybrid and Onsite Options) Full-time. 5+ years experience in a medical device or IVD regulatory affairs role, preferably in molecular diagnostics.
$177,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A law firm is seeking an Assistant General Counsel to manage discovery and records related to firm matters, with a primary focus on client file transfers and legal affairs. Juris Doctor (JD) degree from an ABaccredited law school.
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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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Excellent employment opportunity for a CMC Regulatory Affairs, Data Entry in the Foster City, CA area. Top 3 Nice to Have Skills: Basic understanding of Regulatory Affairs; scientific background preferred; biologics experience is a plus.
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Forms cross-functional alliances with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs, Quality Control and Manufacturing Operations by providing SMEs to these functions and project teams.
$286,220 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The (Sr.) VP/Head of Regulatory Affairs will lead the company’s regulatory strategy and operations. Establish and maintain regulatory affairs systems, ensuring accurate record-keeping and data management.
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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.
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Oversee medical and scientific review of promotional materials for GRC and MRC.Other activities, as assigned, to support LIFE Medical Affairs. Preferred experience in Medical Affairs and/or Clinical Research including Phase IIIb and IV studies; clinical trials management, medical monitoring and scientific expertise.
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affairs job Title: affairs specialist Company: Parexel in Belmont, CA
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