• 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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  • Medical Director , Gastroenterology, MD

    Pfizer (Cambridge, MA)
    …Dir, Rheumatology will be an integral member of the GI/Biosims/Rheum Medical Affairs team supporting current in-line assets (Xeljanz, Inflectra, and Abrilada), as ... well as pipeline assets depending on business needs and priorities. The Director will develop long-term relationships with a wide variety of key healthcare… more
    Pfizer (08/15/25)
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  • Head of Product Quality & Lifecycle Management,…

    Takeda Pharmaceuticals (Lexington, MA)
    …liaison between Biologics Business Unit senior management and Global Quality, Regulatory Affairs , and Operations, fostering seamless communication and decisive ... and processes + Broad knowledge and experience within the GMP environment, and regulatory affairs + Thorough understanding of applicable regulations and guidance… more
    Takeda Pharmaceuticals (07/30/25)
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  • Development Scientific Director , Neurology…

    Sanofi Group (Cambridge, MA)
    …Research Director , Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs , Biostatistics, Clinical Study Units, Medical Affairs ... **Job Title:** Development Scientific Director (DSD) **Location:** Cambridge, MA, **About the Job**...to the protocol development, study feasibility and risk assessment, regulatory submissions, protocol training, scientific review of data, and… more
    Sanofi Group (08/21/25)
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  • Associate Director , US Publications

    Takeda Pharmaceuticals (Lexington, MA)
    …of my knowledge. **Job Description** About the role: Join Takeda as an Associate Director , US Publications where you will work with Director , US Publications and ... and Global functional groups such as Medical, Publications, Medical Information, Regulatory , Statistics, and Legal. * Provide support to respective Product Medical… more
    Takeda Pharmaceuticals (07/30/25)
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  • Director of Public Policy

    State of Massachusetts (Boston, MA)
    …its government relations and policy agenda. As a key member of the External Affairs team, the Director will lead initiatives that shape legislation, advocate for ... and coalition-building, who thrives in a collaborative, mission-driven environment. The Director of Public Policy will work closely with other state agencies… more
    State of Massachusetts (07/03/25)
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  • Sr. Director , Global Market Access…

    Sanofi Group (Cambridge, MA)
    … etc.) + Partner effectively with relevant departments (eg Commercial, Clinical Development, Regulatory Affairs , Medical Affairs , HEOR ) to influence the ... **Job Title:** Sr. Director , Global Market Access and Pricing Lead -...with: + GPT members (NPP/GBL, GPH, GPM, Clinical leads, Regulatory Affairs leads, Medical ) + HEVA… more
    Sanofi Group (07/23/25)
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  • Director , Patient Services and HUB

    Sumitomo Pharma (Boston, MA)
    …seeking a highly motivated and experienced individual for the position of ** Director , Patient Services** . Primary responsibilities include leading and developing a ... strategic framework for patient support services, aligned with brand imperatives. The Director has oversight of patient services operations and manages within the… more
    Sumitomo Pharma (08/15/25)
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  • Director of Pharmacy Benefit Manager…

    State of Massachusetts (Boston, MA)
    …of Insurance ("DOI"), an Agency within the Office of Consumer Affairs and Business Regulation, administers the Commonwealth's insurance consumer protection laws ... their skills and talents to serve our citizens. *_About the Role:_* The Director of Pharmacy Benefit Manager Oversight operating within the Health Care Access Bureau… more
    State of Massachusetts (08/21/25)
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  • Senior Director , Clinical Research,…

    Merck (Boston, MA)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director more
    Merck (08/14/25)
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