• Global Medical Director - Hemophilia

    Sanofi Group (Cambridge, MA)
    …management, politically astute and role model teamwork and collaboration. + Highest ethical, regulatory and scientific standards. **Why Choose Us** + Bring the ... **Job title** : Global Medical Director Hemophilia **Location:** Cambridge, MA / Morristown, NJ...+ Accountable for implementing stakeholder engagement, medical education, and scientific communication plans aligned with the strategic priorities of… more
    Sanofi Group (09/12/25)
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  • Director , Data Science

    Rhythm Pharmaceuticals (Boston, MA)
    …collaboratively with key inter-disciplinary stakeholders (eg biostatistics, clinical development and regulatory affairs ) to drive the generation of actionable ... Summary We are seeking a highly motivated and experienced Director of Data Science to lead data-driven initiatives in...to lead data-driven initiatives in support of our clinical, regulatory , and scientific objectives. The successful candidate… more
    Rhythm Pharmaceuticals (10/22/25)
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  • Associate Director , Biostatistics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex analysis issues, ... team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + Familiar… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Associate Director , Global Labeling Lead

    Takeda Pharmaceuticals (Boston, MA)
    regulatory requirements and guidelines. + Knowledge of other relevant regional regulatory nuances and requirements. + Knowledge of scientific principles and ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
    Takeda Pharmaceuticals (11/23/25)
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  • Director , Global Market Access and Pricing…

    Sanofi Group (Cambridge, MA)
    …, etc.) + Partners effectively with relevant departments (eg Commercial, Clinical Development, Regulatory Affairs , Medical Affairs , HEOR, etc.) to influence ... **Job Title:** Director , Global Market Access and Pricing Strategy -...GMAX CoE, Affiliates ) and beyond (Commercial, Clinical, Medical, Regulatory , Biostatistics, etc.) to build successful access and pricing… more
    Sanofi Group (11/08/25)
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  • Associate Director , Marketing - Care…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Marketing - Care Pathway Education T1D **Location:** Remote/Field **About the Job** The Associate Director , Marketing - Care ... across endocrinology, primary care, and health system settings. The Associate Director will translate brand vision into scalable field enablement resources and… more
    Sanofi Group (10/09/25)
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  • Director , External Research Programs

    Olympus Corporation of the Americas (Westborough, MA)
    …+ Strong cross-functional collaboration experience, including working with Legal, Compliance, Regulatory , Medical Affairs , and Clinical Operations. + Familiarity ... scientists and ensures that external research activities are executed with scientific rigor and operational excellence, while also establishing and refining the… more
    Olympus Corporation of the Americas (11/26/25)
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  • Principal Medical Director , Product…

    Genentech (Boston, MA)
    … will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs , and product development, to ensure the successful ... join the Cardiovascular, Renal, and Metabolism group. The role of Principal Medical Director will focus on guiding the development of our CVRM portfolios. The ideal… more
    Genentech (09/12/25)
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  • Executive Director , Global Program Lead…

    Bristol Myers Squibb (Cambridge, MA)
    …Leadership organization are strategic-thinking, problem-solving, and action oriented scientific leaders who bring drug development and commercialization insights ... late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision… more
    Bristol Myers Squibb (11/20/25)
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  • Director , Global Program Management…

    Takeda Pharmaceuticals (Boston, MA)
    …functions across Takeda Oncology including Translational Medicine, Clinical Sciences, Global Regulatory Affairs , the Oncology Business Unit (Commercial and ... and empower you to shine? Join us as a Director , Global Program Management in our Cambridge office. At...external diagnostic partners, and supporting health authority meetings and regulatory submissions (PMAs etc). This role will partner closely… more
    Takeda Pharmaceuticals (10/28/25)
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