• Associate Director , Scientific…

    Takeda Pharmaceuticals (Boston, MA)
    …and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Scientific Communications Group Lead, Hematology. ... development of scientific communications strategy and deliverables, the **Associate Director , Scientific Communications Lead, Hematology** proactively defines and drives… more
    Takeda Pharmaceuticals (07/02/25)
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  • Water Quality & Regulatory

    Veralto (MA)
    **Water Quality & Regulatory Affairs ...+ Health benefits + Pension Plan Reporting to the Director , Innovation & Product Planning, the Regulatory ... external collaborations, and a proven track record in shaping regulatory frameworks. This position is part of the Innovation...Trojan Technologies is proud to part of the Water Quality segment of Veralto (NYSE: VLTO), a $5B global… more
    Veralto (08/15/25)
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  • Manager of Business & Regulatory

    Beth Israel Lahey Health (Boston, MA)
    …you're making a difference in people's lives.** The Manager of Business and Regulatory Affairs oversees financial performance, regulatory compliance, and ... agencies (CMS, UNOS/OPTN, SRTR) as well as annual updates. 11. Manages regulatory /QAPI process including workgroups to supports transplant quality projects with… more
    Beth Israel Lahey Health (08/08/25)
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  • Manager of Faculty Affairs

    Dana-Farber Cancer Institute (Boston, MA)
    The Manager of Faculty Affairs at Dana-Farber Cancer Institute (DFCI) plays a pivotal role in the administration of faculty affairs within the joint clinical ... This position is responsible for overseeing all aspects of the faculty affairs process, from managing faculty position creation, searches, on- and off-boarding,… more
    Dana-Farber Cancer Institute (08/26/25)
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  • Associate Director , Regulatory

    Rhythm Pharmaceuticals (Boston, MA)
    …across functions, and ensuring quality , accuracy, and adherence to regulatory guidelines. Additionally, the Associate Director supports the preparation and ... or related field + 8+ years of highly relevant pharmaceutical/biotechnology experience in Regulatory Affairs Operations + Knowledge and understanding of the drug… more
    Rhythm Pharmaceuticals (07/30/25)
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  • Director , Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for ... regulatory nuances and requirements. + Understanding of scientific principles and regulatory / quality systems relevant to drug development. + Ability to… more
    Takeda Pharmaceuticals (08/31/25)
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  • Associate Director , Product Quality

    AbbVie (Waltham, MA)
    …Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , R&D, and S&T to ensure alignment on strategic ... Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , Research and Development. Additional Information Applicable… more
    AbbVie (07/11/25)
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  • Associate Director , Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... auditing and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high- quality standards, this role supports… more
    Takeda Pharmaceuticals (07/25/25)
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  • Global Medical Director , Evidence…

    Sanofi Group (Cambridge, MA)
    …+ Collaborate with glocal cross-functional teams including Medical TA, Clinical Development, Regulatory Affairs , HEVA, Market Access, and Commercial to align ... **Job title** : Global Medical Director , Evidence Generation - Innovation & Partnerships **Location:**...engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs more
    Sanofi Group (07/23/25)
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  • GRA Device Lead ( Director )

    Sanofi Group (Cambridge, MA)
    …within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research ... and Development. Sanofi's global regulatory affairs (GRA) function is comprised of...key stakeholders including clinical, medical affairs , Industrial Affairs (Device Development, manufacturing, quality , supply chain)… more
    Sanofi Group (07/15/25)
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