• Senior Interpreter

    University of Texas Rio Grande Valley (Edinburg, TX)
    …must have prior approval from the VP of HR & Regulatory Affairs . Quick Linkhttps://careers.utrgv.edu/postings/49210 Posting Supplemental Questions Required ... with SAS team regarding accommodation services, case management, and program development. Reviews documentation and recommends appropriate accommodations on an… more
    University of Texas Rio Grande Valley (10/31/25)
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  • Senior Clinical Trial Coordinator

    Olympus Corporation of the Americas (Center Valley, PA)
    …tracking, review, and collection of study-specific documents required in the site's Regulatory Binder. + Assist in tracking study activies and milestones by managing ... coverage effective on start date + 24/7 Employee Assistance Program + Free live and on-demand Wellbeing Programs +...state or local law. Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Medical Affairs more
    Olympus Corporation of the Americas (10/23/25)
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  • Executive Director, Therapeutic Areas

    Taiho Oncology (Princeton, NJ)
    …guidelines. + Partners with the Clinical Development, Product Development, Regulatory Affairs , Commercial, Legal and Finance departments. Education/Certification ... Employee Value Proposition: This role provides the opportunity to lead Medical Affairs (MA) activities across therapeutic areas for both pipeline and marketed… more
    Taiho Oncology (11/05/25)
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  • Group Lead, Global Scientific Communications,…

    Takeda Pharmaceuticals (Cambridge, MA)
    …when applicable through close collaboration with cross-functional teams (including Medical Affairs , Clinical Development, Regulatory Affairs , Commercial, GPD ... Expertise:** + Comprehensive understanding of the pharmaceutical industry and medical affairs + Global regulatory expertise with demonstrated strong ability… more
    Takeda Pharmaceuticals (10/23/25)
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  • Program Associate, Bureau of Tuberculosis…

    City of New York (New York, NY)
    …teams involved in critical areas like drug-resistant TB case management and regulatory affairs . This position requires a highly organized, detail-oriented, and ... and manage correspondence; take clear and concise meeting minutes. - Assist the Regulatory Affairs Coordinator: Support the preparation and review of … more
    City of New York (11/19/25)
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  • Governance Risk and Control - Regulations…

    Citigroup (Tampa, FL)
    …Policies. + Contribute to the oversight of the MCA program , including the annual/semi-annual/quarterly/monthly attestation, quality oversight, and related reporting. ... enabling better management and decision-making in line with the expectations of senior management, Board, and Regulators. + Be involved in operations of Citi's… more
    Citigroup (11/26/25)
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  • Executive Director, Global Program Lead…

    Bristol Myers Squibb (Cambridge, MA)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Global Program Leads within the ICV Global Program Leadership ... late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision… more
    Bristol Myers Squibb (11/20/25)
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  • Program Manager - Research Compliance

    Dartmouth Health (Lebanon, NH)
    …and manages Research Quality & Safety initiatives relating to research compliance, regulatory affairs , and the protection of the rights, safety, welfare ... * Coordinates and conducts Research Quality & Safety human subject research, regulatory affairs and research compliance educational initiatives. * Presents and… more
    Dartmouth Health (12/12/25)
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  • Product Licensing Director

    GE Vernova (Wilmington, NC)
    …Licensing Director will help establish and implement the product strategy for Regulatory Affairs , including new plant deployment, proposals for regulatory ... and deployment for GVH product licensing. + Implement the vision of the Regulatory Affairs and Licensing organization to support Business objectives through… more
    GE Vernova (11/18/25)
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  • Associate Director, Clinical Research (US Remote)

    Terumo Neuro (Aliso Viejo, CA)
    …priorities. + Act as a key liaison between Clinical Operations and departments such as Regulatory Affairs , Quality, R&D, PACE, R&D, and Medical Affairs to ... study management, team leadership, and strong cross-functional collaboration with Medical Affairs , PACE, Regulatory , Clinical Safety, and Data Management. Ensure… more
    Terumo Neuro (11/21/25)
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