• Associate Director , Contract…

    Sumitomo Pharma (Boston, MA)
    …https://www.us.sumitomo-pharma.com or follow us on LinkedIn. **Job Overview** The ** Associate Director , Commercial Drug product Manufacturing and Packaging** ... assigned projects to coordinate technology transfer and development efforts per project milestones, timelines, and deliverables for projects. + Reviews and… more
    Sumitomo Pharma (11/19/25)
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  • Associate Director , Global Health…

    Takeda Pharmaceuticals (Boston, MA)
    …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... Market Access, Global Evidence and Outcomes, Medica Affairs, Clinical Development, Regulatory Affairs, Biostatistics, Global Emerging Markets (GEM; eg, China), … more
    Takeda Pharmaceuticals (09/30/25)
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  • Associate Director , Oncology…

    Bristol Myers Squibb (Cambridge, MA)
    …to regulatory submissions. This individual will work on cross-functional project teams to drive execution of translational/biomarker plans working with disease ... with Biomarker Lead late stage clinical trials for Phases II/III preferred. Regulatory submissions drug approvals in solid tumor space also highly desirable.… more
    Bristol Myers Squibb (11/08/25)
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  • Associate Director - Clinical…

    Lilly (Boston, MA)
    …studies from planning to close-out, ensuring adherence to timelines, budgets, and regulatory guidelines (FDA, EMA, GCP, ICH) using a risk-based approach. + Develop ... alignment with company goals. + Partner with cross-functional teams (eg, Clinical, Regulatory , Supply Chain) to support the strategic development and execution of… more
    Lilly (10/31/25)
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  • Associate Director , Global Evidence…

    Takeda Pharmaceuticals (Boston, MA)
    …analysis plans, scientific reports, briefing packages, clinical study reports, and regulatory labelling interactions. + Provide technical expertise and guidance on ... providers and payers. + Provides input into clinical development, regulatory , reimbursement documents. + Performs/manages, as appropriate, relevant research… more
    Takeda Pharmaceuticals (10/29/25)
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  • Associate Director , Statistical…

    Sumitomo Pharma (Boston, MA)
    …of the problems. + Act as a liaison between statistical programming, subcommittees and project teams as + undefined + May serve as an external spokesperson for the ... using SAS + Ability to generate documents / files required for regulatory filing. Ex. Reviewers' Guides, Define.XML, Annotated CRFs etc. + Executing Pinnacle… more
    Sumitomo Pharma (10/08/25)
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  • Associate Director : Tumor Biology…

    Takeda Pharmaceuticals (Boston, MA)
    …with urgency and excellence + Serve as senior scientific advisor and project lead, providing technical guidance to teams and stakeholders. + Represent Takeda ... + Maintain robust documentation (eg, Electronic Lab Notebooks) and support regulatory submissions. + Mentor and develop scientific talent, fostering innovation,… more
    Takeda Pharmaceuticals (10/05/25)
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  • Associate Director , Statistics…

    Takeda Pharmaceuticals (Boston, MA)
    …clinical + Facilitate execution and delivery collaboration cross functionally in Global Project Teams (GPTs), generally within DQS and R&D, and with external vendors ... industry standards applicable to the design, analysis of clinical trials and regulatory submissions. + Strong statistical programming skills + Excellent oral and… more
    Takeda Pharmaceuticals (09/20/25)
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  • PCO Medical Director - UM - Full Time

    CenterWell (Boston, MA)
    …a part of our caring community and help us put health first** The Medical Director , Primary Care relies on medical background and reviews health claims. The Medical ... Director , Primary Care work assignments involve moderately complex to...be authorized. All work occurs with a context of regulatory compliance, and work is assisted by diverse resources… more
    CenterWell (11/06/25)
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  • Executive Director - Massachusetts State…

    State of Massachusetts (Boston, MA)
    …against licensees who engage in professional misconduct when necessary. The Executive Director ("ED") for MSAC reports to the Associate Deputy Commissioner ... Provide written and oral advice to the Agency on regulatory matters related to MSAC. * Establish and maintain...records unit with filling these requests. * Assist the Director of External Affairs and the OCA Legislative Liaison… more
    State of Massachusetts (09/19/25)
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