• Senior Director , Global Regulatory Lead,…

    Takeda Pharmaceuticals (Boston, MA)
    …+ Advanced degree in a scientific discipline (PharmD/PhD/MD) strongly preferred + 12+ years of pharmaceutical industry experience. This is inclusive of 10 ... advice to teams to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. +… more
    Takeda Pharmaceuticals (08/20/25)
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  • Director , Sustainability Enablement

    Bristol Myers Squibb (Devens, MA)
    …line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance ... career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety… more
    Bristol Myers Squibb (09/05/25)
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  • Clinical Research Director , Neurology…

    Sanofi Group (Cambridge, MA)
    …clinical research experience in Alzheimer's disease is highly desired. + Understanding of pharmaceutical product development and life cycle management gained ... **Job Title:** Clinical Research Director **Location:** Cambridge, MA, **About the Job** Are...budget, and contingency/risk management plans to assure successful execution of the clinical trials in compliance with… more
    Sanofi Group (08/21/25)
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  • USMA Regional Medical Scientific Director

    Merck (Boston, MA)
    **Job Description** **Position Responsibilities** + The Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and ... disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual,… more
    Merck (09/05/25)
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  • Associate Director , Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and Device ... degree with 15+ years of experience** + Minimum 5 years of combination product, medical device, or pharmaceutical industry experience + Experience… more
    Takeda Pharmaceuticals (09/04/25)
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  • Associate Director , Global Regulatory…

    Sanofi Group (Cambridge, MA)
    …record with a minimum of 1 year (3+ years preferred) of regulatory experience, preferably within the pharmaceutical /medical device/biotech industry + ... **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location**...scientific subject matter is extremely helpful + Significant understanding of the US pharmaceutical marketplace, especially the… more
    Sanofi Group (08/12/25)
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  • Associate Director , MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …This role is responsible for ensuring the robustness, scalability, and compliance of downstream operations through effective technology transfer, validation ... **Job Summary** **​** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director , MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …skilled and experienced professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. ... This role is responsible for ensuring the robustness, scalability, and compliance of upstream operations through effective technology transfer, validation… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Director , Quantitative Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment ... application is true to the best of my knowledge. **Job Description** Are you looking for...and empower you to shine? Join us as a Director , Quantitative Clinical Pharmacology Lead in our Cambridge, MA… more
    Takeda Pharmaceuticals (06/11/25)
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  • Associate Director , Third Party…

    AbbVie (Waltham, MA)
    …+ Strong strategy development and planning skills coupled with necessary knowledge of pharmaceutical development, manufacturing and supply activities. + Issue ... product and maximizes profitability throughout its life cycle. Through matrix management of cross functional groups/individuals, the Associate Director , TPM is… more
    AbbVie (09/05/25)
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