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Interface broadly with key functions including Discovery Sciences, Preclinical Pharmacology, Pharmaceutical Sciences, Toxicology, Translational Biomarkers, Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late stage Clinical Research throughout sites in the USA, UK and Belgium.
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Reports to: Executive Vice President and Managing Director, Chief Counsel, Head of Global Regulatory Affairs. Position Title: Counsel/Senior Counsel, Regulatory Affairs (position title and compensation is commensurate with experience.
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10+ years of prior working experience in electric regulatory affairs and policy advocacy required, preferably in the ERCOT region. Hunt Energy Network (HEN) is seeking a highly motivated, trustworthy individual with experience working independently to serve as HEN's Director of Regulatory Affairs.
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Experienced HireShift 1 (United States of America)US, Washington, D.C.Intel’s Legal, Trade, and Government Affairs (LTG) group offers unique opportunities to work in a variety of areas, including counsel to Intel businesses; technology and intellectual property licensing; patent prosecution; trademarks and brands; litigation, mergers, acquisitions and investing; public policy, legislative and regulatory lobbying; global trade, export, import, and customs; and corporate compliance.
$162,600 - $284,620 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Effectively represent the Global Regulatory Affairs (GRA) function in senior-level interactions at internal governance technical review committees, key global health authority meetings, and external partners.
$165,200 - $236,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Reporting to the Director in Regulatory Chemistry, Manufacturing & Controls (CMC), the Senior Scientist is responsible for implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned products in accordance with global regulations, guidance's, and defined regulatory strategies.
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A thorough understanding of the complex Regulatory, Development and Medical Affairs requirements in oncology, as well as the emerging paradigm for cell & gene therapySelf-organizer, meticulous hands-on habits, keen attention to detail.
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At least 5 years’ experience in regulatory affairs working on a range of nutritional products (common general foods, food/dietary supplements, infant formula/baby food, medical food) on the US market.
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Support the IT and Medical Affairs teams with healthcare regulatory matters and third party contracting. Serve as the lead attorney for the company’s Value-Based Care business unit advising the VBC leadership team on legal and regulatory matters, risk management strategies, and contracting strategies.
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The Director, Corporate Counsel – Rare Disease will serve as the legal advisor to the US Commercial, Patient Advocacy, Public Affairs, Regulatory, and Medical Affairs teams supporting our Rare Disease Franchise, and will coordinate legal services with the attorney responsible for Canadian support for the Rare Disease Franchise.
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As The Focus Of This Internship, We Would Like To Study The Potential For How Generative AI Can Be Used In The Drug Development Lifecycle To Accelerate The Approach To Areas Such As Regulatory Filings, Generation Of Real World Evidence, Clinical Trial Documentation And Audits.
$10,120 - $12,170 a yearInternExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Evaluate the development of regulatory frameworks in health and life sciences, particularly as related to the use of AI to generate real world evidence, to educate a diverse audience and facilitate discussions about the impact of regulation on our work.
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From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.
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Supports Regulatory Affairs with regulatory agency submissions for new product development by providing clinical trial data review, synopses, and reports for those submissions. Regulatory Compliance: Performs Institutional Review Board (IRB) submission efforts related to LifeNet Health research and development team determinations.
$111,170 - $185,284 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Analyst II, Regulatory Affairs has experience with and performs key centralized complex and difficult regulatory activities for the Compliance Department. Knowledge of and experience with state and Federal regulatory and other requirements and practices related to Covered California, Medicare and Medi-Cal (Medicaid), Title 19 (USC)/Title 29 (USC and CCR), Title 22 (CCR), Title 28 (CCR), Title 42 (USC and CFR), CA Welfare and Institutions Code, and CA Health and Safety Code.
$33.66 - $42.92 an hourFull-timeExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: assistant Company: Veterans Canteen Service
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