• Associate Director , Clinical PV…

    Takeda Pharmaceuticals (Boston, MA)
    …in the business units and affiliates. + Ensure that the Global Quality Audit functions consider clinical research and pharmacovigilance regulated activities ... **OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business… more
    Takeda Pharmaceuticals (12/12/25)
    - Related Jobs
  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ... functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and… more
    Takeda Pharmaceuticals (11/14/25)
    - Related Jobs
  • Associate Director , Rare Blood…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Rare Blood Disorders, Patient Services **Location:** Cambridge, MA **About the Job** Join the team transforming care for ... patients with some of the highest unmet needs. The Associate Director , Sutimlimab Patient Solutions will report...implementing services and education, how we can increase the quality and efficiency of these services. They will need… more
    Sanofi Group (11/20/25)
    - Related Jobs
  • Associate Director , GCP Audit…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight to clinical, ... leadership, supplier oversight, and strategic risk management to enhance end-to-end clinical quality . **HOW YOU CONTRIBUTE** + Lead strategic quality oversight… more
    Takeda Pharmaceuticals (11/21/25)
    - Related Jobs
  • Associate Director , Regulatory…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... intelligence management Standard Operating Procedures or work practices. + Review overall quality of ad hoc query research for requested regulatory topics and… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
    - Related Jobs
  • Associate Director , Statistics

    Takeda Pharmaceuticals (Boston, MA)
    …Quantitative Sciences, Programming, Global Evidence Outcomes, Patient Safety & Pharmacovigilance , and Strategic Operations The department integrates data science, ... efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and pursue operational excellence. **Delivery & Business… more
    Takeda Pharmaceuticals (12/11/25)
    - Related Jobs