• Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory...changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues… more
    Takeda Pharmaceuticals (06/07/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    … requirements. You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead...+ Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts… more
    Takeda Pharmaceuticals (06/07/24)
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  • Associate Director , US Advertising…

    Sanofi Group (Cambridge, MA)
    **Job title: Associate Director , US Advertising and Promotion, Global Regulatory Affairs ** + Location: Cambridge, MA or Bridgewater, NJ **About the ... job** The Associate Director , US Advertising and Promotion serves... lead on Review Committees (RCs). As the RC Regulatory Affairs representative, work with brands on… more
    Sanofi Group (06/19/24)
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  • Director Regulatory Affairs

    Merck (Boston, MA)
    …Product Development Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external ... world. **Looking for someone with a growth mindset. The Director , Regulatory Affairs Liaison is... regulatory agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or… more
    Merck (05/22/24)
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  • Senior Manager RA , Global Reg…

    AbbVie (Waltham, MA)
    …multiple driver indications within a Therapeutic Area and supports the Manager ( Global Regulatory Lead (GRL), Associate Director , or Director ), in ... Advise internal customers who may contribute to regulated communication on Regulatory /FDA issues including Public Affairs , Clinical Development, Legal, and… more
    AbbVie (06/19/24)
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  • Device Regulatory Lead ( Associate

    Sanofi Group (Cambridge, MA)
    …+ Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global Regulatory Affairs Device team is a globally diverse team ... **Job title: Device Regulatory Lead ( Associate Director )**...portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory more
    Sanofi Group (06/06/24)
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  • Senior Clinical Director , Immunology

    Merck (Boston, MA)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... regulatory filing, and publication. **Specifically, The Senior Clinical Director May Be Responsible For:** + Evaluating pre-clinical and translational work… more
    Merck (05/25/24)
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  • Contract Center Medical Director /Center…

    CSL Plasma (East Providence, RI)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... as or delegates to another appropriate physician the duties of "laboratory director ", "technical consultant", or "clinical consultant" as prescribed by the Clinical… more
    CSL Plasma (04/16/24)
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  • Law Fellow

    Fresenius Medical Center (Waltham, MA)
    …on projects with other FME departments including Compliance, Regulatory Affairs , Clinical Services, the Medical Office, Global IP, and others. ... manufacturers, and related entities. Under the general supervision of an Associate General Counsel or his/her designee, the Fellow undertakes projects supporting… more
    Fresenius Medical Center (06/08/24)
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  • Medical Writer

    Novo Nordisk (Lexington, MA)
    …personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs , Global Safety, Data Management, and ... the written deliverables that support the clinical development and regulatory requirements of a clinical program. The Medical Writer...personnel. Relationships The Medical Writer (MW) reports to an Associate Director of Medical Writing. The MW… more
    Novo Nordisk (06/14/24)
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