• Senior Regulatory Affairs…

    Hologic (Marlborough, MA)
    Senior Regulatory Affairs Specialist Newark, DE, United States Marlborough, MA, United States United States **Join us as a Regulatory Affairs ... with R&D, Quality, Clinical, and Marketing, you will prepare and manage regulatory submissions , technical files, and documentation to meet US, EU, and Canadian… more
    Hologic (07/19/25)
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  • Sr. Regulatory Affairs Specialist

    Medtronic (Mansfield, MA)
    …innovation in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for ... requirements + Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and… more
    Medtronic (07/01/25)
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  • Sr. Regulatory Affairs Specialist

    ConvaTec (Lexington, MA)
    …departments including but not limited to QC and legal in order to support regulatory submissions . **Travel Requirements** Position may involve travel up to 25% ... regulations and guidance documents to ensure complete and scientifically sound product submissions , as required. + Generate and execute regulatory strategies for… more
    ConvaTec (08/02/25)
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  • Senior Manager, Business Development

    The Brattle Group (Boston, MA)
    …Group, a privately held, global economics consulting firm, is looking for a ** Senior Manager, Business Development** to join either our **Boston, New York, or San ... and collaboration to advance the program and function we are building. The Senior Business Development Manager (BDM) works directly with the Managing Group Leader… more
    The Brattle Group (06/11/25)
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  • Senior Clinical Research Director, I&I

    Sanofi Group (Cambridge, MA)
    …structure of the clinical sections of the BLA/CTD, Briefing packages for regulatory meetings, PSP/PIP Supports registrations, label submissions and modifications ... you thought was possible. Ready to get started? The Senior Clinical Research Director (Sr CRD) is noted as...for research projects + Represents his/her project at key regulatory agency meetings as the medical spokesperson for the… more
    Sanofi Group (07/06/25)
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  • Principal Medical Writer

    Sanofi Group (Cambridge, MA)
    …in a timely manner for study start, conduct and completion, as well as regulatory submissions according to company standards and procedures with the ultimate aim ... and Project Team. This is a position for a senior medical writer who has an extensive experience with...extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership skills as submission… more
    Sanofi Group (07/31/25)
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  • Research Administrator II (Post Award)

    Beth Israel Lahey Health (Boston, MA)
    **Overview** **The Senior Research Administrator, Post-Award (Research Administrator II)** will, under the direction of the Director, Major Projects and Post Award ... and translate financial data so it is understandable for the non- specialist . Investigate any anomalies and provides timely resolutions. Reallocate budgets and… more
    Beth Israel Lahey Health (06/25/25)
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