• Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …what is possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is ... responsible for developing innovative global regulatory strategies and providing strategic regulatory guidance...and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
    Takeda Pharmaceuticals (05/07/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director Global Regulatory Lead, GRAD Oncology. You ... **How you will contribute:** + Defines, develops, and leads global strategies to maximize global regulatory...in collaboration with their regional counterparts. + As the Associate Director , you will be responsible for… more
    Takeda Pharmaceuticals (04/15/25)
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  • Global Regulatory Affairs,…

    GRAIL (Washington, DC)
    …and healthcare companies. For more information, please visit grail.com . The Associate Director of Global Regulatory Affairs & Safety serves as a key ... GRAIL's UK Responsible Person (UKRP). Interfaces with MHRA and other International regulatory agencies, Notified Bodies, and external consultants as needed, on IVD… more
    GRAIL (06/17/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …my knowledge. **Job Description** **Objective / Purpose:** + Defines, develops and leads global strategies to maximize global regulatory success towards ... + Provides leadership and development for direct reports, including those that serve as global regulatory leads responsible for the design and execution of … more
    Takeda Pharmaceuticals (05/13/25)
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  • CDx Associate Director

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …partner side) _CDx RA Policy and Intelligence_ : Keep abreast of the changing global regulatory environment for devices and share/educate CDx department on these ... + Understanding of strategic and tactical role and deliverables of Global Regulatory Strategy in the Drug and Device Development and Commercialization process.… more
    Daiichi Sankyo Inc. (05/29/25)
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  • Associate Director , Global

    Bristol Myers Squibb (Princeton, NJ)
    …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** ... **Position Summary:** The selected candidate will have leadership responsibility for global regulatory strategy within a development team (DT). Serve as team… more
    Bristol Myers Squibb (06/05/25)
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  • Associate Director , Global

    Gilead Sciences, Inc. (Foster City, CA)
    …strategy, plans and objectives for assigned products or projects. You may act as the Global Regulatory Lead for early-stage or other programs. You will lead ... Regulatory Affairs and may serve as Regional Lead or Global Regulatory Lead on cross-functional/cross-regional Regulatory Submission Teams. Provides… more
    Gilead Sciences, Inc. (04/11/25)
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  • Associate Director

    Gilead Sciences, Inc. (Foster City, CA)
    …Description** Regulatory Affairs Labeling is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner ... learn new therapeutic areas. + Demonstrates in-depth knowledge of current global and regional trends in regulatory affairs and is able to apply this to advance… more
    Gilead Sciences, Inc. (05/23/25)
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  • Senior Director , Global

    Lilly (Indianapolis, IN)
    …are determined to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA-CMC) leads and ... to lead preparation, review, and finalization of CMC documents for global regulatory submissions, including Clinical Trial Applications, Market Authorization… more
    Lilly (06/25/25)
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  • Manager/ Associate Director

    Boehringer Ingelheim (St. Joseph, MO)
    …such as governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs (RA) core or ... (RA) Pharma Safety & Efficacy will represent the US regulatory safety and efficacy function in global ...as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety… more
    Boehringer Ingelheim (06/22/25)
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