• Clinical Research Director - RBD

    Sanofi Group (Cambridge, MA)
    **Job Title:** Clinical Research Director - RBD **Location:** Cambridge, MA Morristown, NJ **About the Job** Are you ready to shape the future of medicine? The race ... any other characteristic protected by law. The Clinical Research Director (CRD) provides medical and scientific expertise to the...other members of the CDST (ie, GPH, CSO PL, regulatory , statistics, and PM) + The CRD will lead… more
    Sanofi Group (08/25/25)
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  • Associate Director , Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …teams + Serve as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality , and commercial functions + Coordinate ... across multidisciplinary teams to deliver device clinical outcomes that exceed quality benchmarks and regulatory standards. **Core Responsibilities:** **Device… more
    Takeda Pharmaceuticals (06/06/25)
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  • Associate Director , Global Regulator…

    Bristol Myers Squibb (Cambridge, MA)
    …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
    Bristol Myers Squibb (08/28/25)
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  • Assistant Director , Student Services,…

    Boston University (Boston, MA)
    **ASSISTANT DIRECTOR , STUDENT SERVICES, International Students and Scholars Office** **Job Description** **ASSISTANT DIRECTOR , STUDENT SERVICES, International ... as they apply for immigration benefits. 30% Coordinate with the Associate Director on the development of university policies and procedures related to processing… more
    Boston University (08/02/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …Collaborate cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other ... **Associate Director , Small Molecule Analytical Development** + Lead and...the drug development lifecycle, including preclinical and clinical stages, regulatory requirements, and quality standards. **Competencies** **Accountability… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Associate Director , Commercial Engagements…

    Takeda Pharmaceuticals (Cambridge, MA)
    …and policies. + Collaborate with internal cross-functional stakeholders (Marketing, PRT, Medical Affairs , Legal, Regulatory , Ethics & Compliance) to ensure the ... the best of my knowledge. **Job Description** **About the role:** The Associate Director , Commercial Engagements & P2P Strategy, offers a unique opportunity to shape… more
    Takeda Pharmaceuticals (08/08/25)
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  • Clinical Research Director , I and I,…

    Sanofi Group (Cambridge, MA)
    …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing + ... **Job title** : Clinical Research Director , I and I, Pulmonology **Location:** Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The… more
    Sanofi Group (08/30/25)
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  • Clinical Research Director

    Sanofi Group (Cambridge, MA)
    …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing. + ... **Job Title:** Clinical Research Director **Location** : Morristown, NJ Cambridge, MA **About the Job** Ready to push the limits of what's possible? Join Sanofi in… more
    Sanofi Group (08/22/25)
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  • Medical Director , Gastrointestinal…

    Takeda Pharmaceuticals (Boston, MA)
    …and communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , ... strategy for and lead preparation of responses to safety-related inquiries from regulatory agencies and ethics committees. + Ensure communication of all safety… more
    Takeda Pharmaceuticals (08/31/25)
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  • Senior Director , MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …cost reduction where appropriate. + Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership...validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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