• Regulatory Strategist

    Sanofi Group (Cambridge, MA)
    …of relevant pharmaceutical/biotechnology experience, including at least 4 years of relevant Regulatory Affairs experience (regional and global), in early and ... **Job Title:** Regulatory Strategist **Location:** Morristown, NJ/Cambridge, MA **About the...accelerate progress. As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global… more
    Sanofi Group (07/30/25)
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  • MassHealth Regulatory Compliance & Audits…

    Commonwealth Care Alliance (Boston, MA)
    …field preferred. Required Experience (must have): * 5+ years in healthcare compliance, regulatory affairs , or claims audit. * Experience working with TPA ... to the Director, Claims Operations & Quality Assurance, the Regulatory Compliance & Audits Sr. Specialist II is responsible...track system change requests, and prepare for audits and regulatory reviews. This role is critical to supporting CCA's… more
    Commonwealth Care Alliance (06/02/25)
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  • Sr. Coordinator, Regulatory Submission…

    Cardinal Health (Boston, MA)
    **_What Regulatory Submissions Operations contributes to Cardinal Health_** Regulatory Submissions Operations provides regulatory affairs and product ... services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. More specifically, this role serves the function to support… more
    Cardinal Health (08/13/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Boston, MA)
    …budget for Oncology clinical development activities. + Partner with Translational Research, Regulatory Affairs , Clinical Operations, and Medical Affairs to ... submissions, clinical study reports, and NDA/MAA filings. + Collaborate with regulatory affairs team to ensure compliance with regulatory requirements. **Key… more
    Sumitomo Pharma (08/14/25)
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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 more than 1800 people. The GRA Device Lead for Specialty Care Combination… more
    Sanofi Group (07/15/25)
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  • Global Medical Director, Evidence Generation…

    Sanofi Group (Cambridge, MA)
    …+ Collaborate with glocal cross-functional teams including Medical TA, Clinical Development, Regulatory Affairs , HEVA, Market Access, and Commercial to align ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs to develop and launch first in class and best… more
    Sanofi Group (07/23/25)
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  • Chief Medical Officer

    Beth Israel Lahey Health (Plymouth, MA)
    …latest trends in field of expertise especially related to health care quality, regulatory affairs , organizational behavior and leadership + Performs all duties ... Plymouth Hospital. The CMO is responsible for the overall medical and administrative affairs related to health care delivery and medical staff management of patient… more
    Beth Israel Lahey Health (07/08/25)
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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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  • Director Medical Writing & Clinical Development

    Philips (Cambridge, MA)
    …including Medical Affairs , Clinical Development, Research & Development, and Regulatory Affairs . + **Develops** clinical evidence strategies for New Product ... a key member of the Ultrasound Medical and Clinical Affairs team and serves as a subject matter expert,...to support medical device performance in alignment with EU regulatory standards (MEDDEV 2.7.1 Rev. 4, EU Medical Device… more
    Philips (07/31/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Boston, MA)
    …global team members, other B&L departments (eg, R&D/Project Management, Clinical/Medical Affairs , Biometrics, Regulatory Affairs , Quality Assurance, ... in an accurate and timely manner. + Provide Clinical Operations support to the Regulatory Affairs department. Leadership: + Manage in-house team of CRAs, CTAs… more
    Bausch + Lomb (06/07/25)
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