• Regulatory Strategist

    Sanofi Group (Cambridge, MA)
    **Job Title:** Regulatory Strategist **Location:** Morristown, NJ/Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The race is on to ... accelerate progress. As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global...in a relevant scientific discipline required. Advanced degree (PharmD, PhD , MD, or DVM or MSc in Biology, Life… more
    Sanofi Group (07/30/25)
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  • Senior Director Global Regulatory Affairs…

    Takeda Pharmaceuticals (Boston, MA)
    …to bring life-changing therapies to patients worldwide. The Senior Global Regulatory Affairs, Neuroscience is responsible for developing innovative global ... regulatory strategies and providing strategic regulatory guidance...Advanced degree in a scientific subject area (eg MSc, PhD , PharmD, MD). BA acceptable with significant Industry experience.… more
    Takeda Pharmaceuticals (07/18/25)
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  • Senior Principal, Regulatory Affairs…

    Danaher Corporation (Boston, MA)
    …which makes everything possible. The Senior Principal, Regulatory Affairs is responsible for regulatory ... and digital pathology in the clinical oncology environment. The Senior Principal, Regulatory Affairs will provide oversight and lead global submission work including… more
    Danaher Corporation (07/09/25)
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  • Associate Director, Global Regulatory

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director, Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** Are ... critical in helping our teams accelerate progress. The Associate Director, Global Regulatory Affairs - Global Labeling Strategy is responsible for leading the… more
    Sanofi Group (06/27/25)
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  • Director, Global Regulatory Affairs…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Director, Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** Are you ready ... be critical in helping our teams accelerate progress. The Director, Global Regulatory Affairs - Global Labeling Strategy is responsible for leading the development… more
    Sanofi Group (06/27/25)
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  • Director, Regulatory Site CMC

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. The Director Regulatory Site CMC ensures efficient and compliant management of regulatory ... management and explores automation to enhance predictability and repeatability in regulatory processes. We are looking for someone with strong practical experience… more
    Takeda Pharmaceuticals (06/04/25)
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  • Senior Associate - Specialist, Global…

    Takeda Pharmaceuticals (Boston, MA)
    …bring life-changing therapies to patients worldwide. Senior Associate - Specialist, Global Regulatory Affairs CMC role is within in the GRA Chemistry Manufacturing & ... functions as follows: + With supervision, support the execution of regulatory CMC investigational, registration and post-approval strategies for assigned products. +… more
    Takeda Pharmaceuticals (08/20/25)
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  • Research Scientist - Regulatory Submission…

    ThermoFisher Scientific (Boston, MA)
    …full-time benefits. **Key responsibilities:** + Support preparation of global regulatory submission sections, for late-stage and commercial programs in analytical ... Perform data verification, trending, and statistical analysis to support regulatory strategy and product characterization. + Collaborate cross-functionally with… more
    ThermoFisher Scientific (06/28/25)
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  • Principal Product Software Engineer AI | Legal…

    Wolters Kluwer (Waltham, MA)
    …to help save lives, improve how we do business, and build better judicial and regulatory systems. We help them get it right. This role is part of the Advanced ... we support, VitalLaw, is trusted by customers to help legal professionals achieve regulatory compliance and better understand complex legal issues in key areas like… more
    Wolters Kluwer (08/15/25)
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  • Senior Medical Director

    Astrix Technology (Boston, MA)
    …programs worldwide. + Ensure adherence to international clinical development and regulatory standards. **Qualifications:** + MD or MD/ PhD with specialization ... including RNA, genomic, proteomic, and imaging-based markers. + Contribute to global regulatory submissions (eg, INDs, CTAs) and provide medical input in alignment… more
    Astrix Technology (08/11/25)
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