• Associate Director , Clinical

    Takeda Pharmaceuticals (Lexington, MA)
    …my employment application is true to the best of my knowledge. **Job Description** ** Associate Director , Clinical Research, Value & Evidence Generation, US ... Medical** **Lexington, MA** **Hybrid** **_OBJECTIVES/PURPOSE:_** Provides clinical project management and leadership to ensure successful operational execution of… more
    Takeda Pharmaceuticals (05/03/25)
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  • Associate Director , Clinical

    Takeda Pharmaceuticals (Boston, MA)
    …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... process in partnership with functional compliance teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ)… more
    Takeda Pharmaceuticals (04/25/25)
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  • Associate Director , Clinical

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... supports Takeda's mission by maintaining high standards of quality and compliance in clinical trials. **How will you contribute:** + Drive the implementation of … more
    Takeda Pharmaceuticals (04/16/25)
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  • Associate Director , Digital Health…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …This is a high-autonomy, high-impact role that blends the best of on-label clinical education, access and reimbursement education, sales, and strategy - designed for ... health care. You will: + **Education with credibility and compassion:** Serve as a clinical expert on the Digital Products and the science of the disease state (eg.… more
    Otsuka America Pharmaceutical Inc. (05/23/25)
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  • Compliance Operations Lead, Associate

    Takeda Pharmaceuticals (Boston, MA)
    …improvement + Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and ... metrics for CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and… more
    Takeda Pharmaceuticals (05/24/25)
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  • Sr. Manager, Project Management in

    Bristol Myers Squibb (Devens, MA)
    …projects on time & within budget. This role will report to the Associate Director , Project Management Office (PMO) and Business Operations. **Shifts Available:** ... to mitigate barriers to improvement efforts. + Aligns with Associate Director of PMO to take action(s)...risk mitigation /contingency plans and escalating early to Digital Transformation Program Leader when necessary. + Prepare and present… more
    Bristol Myers Squibb (05/21/25)
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  • HPC Engineer III

    Novo Nordisk (Lexington, MA)
    …and compute power we make available. Relationships The Engineer III reports to: Associate Director Laboratory IT Internal relationships include IT project groups ... and Cambridge reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct… more
    Novo Nordisk (04/19/25)
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