• Director, Global Clinical

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …as an clinical /medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... Development include the following: + Consults with patients or their representatives, clinical , regulatory , and scientific leaders and thoughtfully applies their… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Associate Director, Patient Advocacy

    Orchard Therapeutics (Boston, MA)
    …the advancement of newborn screening. - Work closely with internal teams, including clinical development, regulatory affairs , diagnostics, medical affairs ... advocacy groups and patients to ensure the patient voice is integrated into clinical development, regulatory and market access discussions. - Build and maintain… more
    Orchard Therapeutics (04/03/25)
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  • Executive Director, Product Development Team…

    Merck (Boston, MA)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects, and ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Atherosclerosis… more
    Merck (05/24/25)
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  • Associate Director, Global Labeling Devices

    Takeda Pharmaceuticals (Boston, MA)
    regulatory requirements. Serve as the expert for device labeling on the global Regulatory Affairs (RA) Sub team and Global Device Sub team (GDT) to ensure ... relationships among functions represented at the Labeling cross functional teams including clinical , safety, medical affairs , and commercial, to ensure the… more
    Takeda Pharmaceuticals (05/28/25)
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  • Associate Director, Global Health Economics…

    Takeda Pharmaceuticals (Boston, MA)
    …and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global Emerging Markets ... Interaction + Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10,… more
    Takeda Pharmaceuticals (04/02/25)
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  • Associate Director, Global Regulator…

    Bristol Myers Squibb (Cambridge, MA)
    …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:**… more
    Bristol Myers Squibb (06/05/25)
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  • Associate Executive Director - Board…

    State of Massachusetts (Boston, MA)
    …of Occupational Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making sure the professionals ... rules and regulations including, when necessary, through disciplinary action. The Associate Executive Director ("AED") assists the Executive Director ("ED") with the… more
    State of Massachusetts (05/19/25)
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  • Senior Director, Clinical Research,…

    Merck (Boston, MA)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
    Merck (05/24/25)
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  • MSL Associate Director - North America

    IQVIA (Boston, MA)
    …presentation, analytical and customer service skills. + An understanding of Medical Affairs and clinical development strategy. Support development and execution ... **MSL Associate Director** We are excited to announce that...within the therapeutic area centers through scientific discussions with clinical physicians, staff and other stakeholders, on behalf of… more
    IQVIA (05/29/25)
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  • Associate Director, Drug Product

    Rhythm Pharmaceuticals (Boston, MA)
    …This individual will collaborate with partners in Supply Chain, Quality Assurance, Regulatory Affairs , Finance and various CRO/CMO's to achieve Rhythm's ... individual to join its team in Boston, Massachusetts. The Associate Director will be the technical lead for Drug...including CMC Drug Substance, Supply Chain Management, Quality, and Regulatory Affairs . + Manages and executes activities… more
    Rhythm Pharmaceuticals (05/13/25)
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