• Associate Director , Thought Leader…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    The Associate Director , TLL, Renal Rare Disease, is a field-based, customer facing, non-sales position on Otsuka's Rare Renal team focused on enhancing and improving ... The TLL will work closely with cross-functional leaders from Marketing, Medical Affairs , Sales, Key Accounts, Market Access, Patient Access and the Renal Leadership… more
    Otsuka America Pharmaceutical Inc. (05/01/25)
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  • Executive Director , Cell Therapy Global…

    Bristol Myers Squibb (Devens, MA)
    …lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Executive Director , Cell Therapy Global Product Quality (CTGPQ) is responsible for ... and above site QA and QC, Internal and External Manufacturing, Regulatory Affairs and Brand teams. The individual provides end-to-end global quality oversight of… more
    Bristol Myers Squibb (05/25/25)
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  • Director , Supplier Relationship Management…

    Takeda Pharmaceuticals (Boston, MA)
    …company to inspire you and empower you to shine? Join us as the Director , Supplier Relationship Management (FSP) based in Cambridge, MA reporting to the Head ... to timely and effective resolution + Work closely with Procurement, Therapeutic Areas, Business Partners, CPO and Study teams to review and drive sourcing strategies… more
    Takeda Pharmaceuticals (04/30/25)
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  • Executive Medical Director , Oncology…

    Takeda Pharmaceuticals (Boston, MA)
    …inspire you and empower you to shine? Join us as a Executive Medical Director , Oncology Clinical Sciences in our Cambridge office. At Takeda, we are transforming the ... external compounds (alliances and in-licensing opportunities) + Primary interface with Medical Affairs team for strategy and to support of product commercial efforts… more
    Takeda Pharmaceuticals (04/29/25)
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  • Associate Director , Quantitative Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …that will inspire you and empower you to shine? Join us as Associate Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. At Takeda, ... excellence and individual achievement. + Participates as a member of Business Development due diligence, when requested. + Contributes to infrastructure initiatives… more
    Takeda Pharmaceuticals (04/29/25)
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  • Director , RA Global Regulatory Lead

    AbbVie (Waltham, MA)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory ... of creative global strategies in line with applicable regulations to achieve business objectives for development and marketed products. When necessary, seeks expert… more
    AbbVie (04/04/25)
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  • Director , Computational Multiomics,…

    J&J Family of Companies (Cambridge, MA)
    …while championing patients every step of the way. We are searching for a ** Director , Computational Multiomics, Neuroscience,** to be located at one of our offices in ... human data resources. + Partner with Clinical Development, Global Regulatory Affairs , Data Science, Patient Reported Outcomes, Statistics and other core functions… more
    J&J Family of Companies (05/09/25)
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  • Associate Director , Global Regulator…

    Bristol Myers Squibb (Cambridge, MA)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The ... BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements**...ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of… more
    Bristol Myers Squibb (05/04/25)
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  • Associate Director , Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the quality ... in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
    Takeda Pharmaceuticals (04/25/25)
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  • Associate Director , Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance ... in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
    Takeda Pharmaceuticals (04/16/25)
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