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Director, CMC Regulatory Affairs. 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.
$100 - $113 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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OPPORTUNITY Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market.
$205,000 - $260,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Living Therapeutics Initiative seeks a highly motivated Regulatory Affairs Senior Manager to manage the regulatory affairs, author and assemble IND applications, and help manage FIH studies advancing UCSF-developed cellular therapy candidates.
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Monitor and analyze regulatory and legislative developments that may impact Walmart Last Mile Delivery gig operations. Develops compelling stories, presentations, and whitepapers that effectively communicate the Last Mile Delivery team's regulatory operational strategic plans, initiatives, and impact.
$90,000 - $234,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Adobe is looking for an experienced and innovative Global Trade Compliance Senior Manager to join our team. Ability to create procedures to interpret and align with regulatory policies, while enabling investigators perform appropriate level of due diligence.
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The primary duties for the Assistant Director, Regulatory and Risk Management position will consist of managing and overseeing the insurance program, risk management, and regulatory compliance with grant, state, local, federal requirements, including but not limited to, the Americans with Disabilities Act (ADA), accessibility, Title VI, Limited English Proficiency (LEP), Disadvantaged Business Enterprise (DBE), Small Business Enterprise (SBE), and third-party labor compliance/prevailing wage.
$164,940.67 - $219,760.94 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Drafting/review and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses) The Senior Clinical Scientist reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.
$159,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Regulatory Manager will focus on monitoring and advocating for market policies that will advance the interests of RWECE within the Western interconnect. The Regulatory Manager is a key role within the RWE Clean Energy (RWECE) Regulatory Team working on Wholesale Markets in the West region.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Develop and integrate timelines and budgets for clinical pharmacology activities with overall company timelines and goals, in close coordination with project management, clinical science, CMC, DMPK, nonclinical development, regulatory affairs and other stakeholders.
$262,000 - $321,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Director/Senior Director, Regulatory Affairs CMC will lead the CMC Regulatory Affairs function and be responsible for planning and executing the CMC regulatory strategies for IDEAYA’s therapeutic development programs.
$227,566 - $309,140 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Allogene.com, and follow @AllogeneTx on X (formerly Twitter) and LinkedIn. About the role: Allogene is seeking a Director of Regulatory Affairs within the Regulatory Strategy group who will manage worldwide interactions and negotiations with regulatory agencies and marketing partners in support of investigational studies, product registrations, and commercial products.
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The Senior Director will report to the Vice President of Commercial Strategy and will create and lead market access strategies and tactics that drive the successful commercialization of atacicept.
Starting at $275,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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New York City (Hybrid On-Site): $236,800 - $270,300 for Sr Director, HR Business PartnerSan Francisco, California (Hybrid On-Site): $250,800 - $286,300 for Sr Director, HR Business Partner.
$150Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Senior Wealth Strategist-Client Sales Director page is loaded. Movement within the organization is encouraged, senior leaders are accessible, and you can take pride in working for a company committed to assisting the communities we serve.
$250Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As a Senior Director of People & Culture, you will work across a variety of innovative projects related to people and culture transformation, workforce transition, operating model evolution, and the future of distributed and equitable work.
$210,000 - $315,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago
Title: senior director regulatory affairs Company: American Osteopathic Association in Brisbane, CA
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