• Associate Director , IT Compliance…

    Sumitomo Pharma (Boston, MA)
    …of early- to late-stage investigational assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For more ... IT systems supporting GxP processes comply with FDA 21 CFR Part 11, EU Annex 11, and other applicable...to late-stage investigational assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients… more
    Sumitomo Pharma (01/10/26)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …area is highly desired. Expertise in global regulatory and compliance requirements for clinical research , including but not limited to US CFR , EU CTD, and ICH ... **Experience:** 10+ years' experience in pharmaceutical industry and/or clinical research organization, including 7+ years clinical study/project management. Experience… more
    Takeda Pharmaceuticals (01/06/26)
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