• Associate Director , GCP

    Takeda Pharmaceuticals (Boston, MA)
    …the best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight to ... (or equivalent). + Minimum 15+ years of experience in GCP /GCLP/GVP Quality or Compliance within the pharmaceutical industry. + Advanced understanding of global… more
    Takeda Pharmaceuticals (11/21/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
    Takeda Pharmaceuticals (11/14/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
    Takeda Pharmaceuticals (10/14/25)
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  • Associate Director -Clinical…

    Philips (Cambridge, MA)
    …of our talented Hospital Patient Monitoring (HPM) Clinical Affairs team, the Associate Director - Clinical Operations, is responsible for day-to-day Clinical ... Management and providing expertise in clinical research process legislation, ICH- GCP guidelines, improving efficiency in clinical execution. **Your role:** +… more
    Philips (11/13/25)
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  • Associate Director , Clinical Site…

    Takeda Pharmaceuticals (Boston, MA)
    …company to inspire you and empower you to shine? Join us as an Associate Director , Clinical Site Startup and Engagement Process Excellence & Delivery based ... Ensure implementation of new/updated processes and technologies are in compliance with quality standards (including ICH, GCP ,...in compliance with quality standards (including ICH, GCP , local regulations and Takeda SOPs). + Ensure that… more
    Takeda Pharmaceuticals (12/05/25)
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  • Associate Director , AI & Data,…

    Guidehouse (Boston, MA)
    …**Clearance Required** **:** None **What You Will Do** **:** We are seeking an experienced Associate Director to join our growing AI and Data practice, with a ... well as for shaping and delivering AI- and data-driven transformations. The Associate Director will oversee cross-functional teams and collaborate directly with… more
    Guidehouse (11/09/25)
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  • Associate Director , Quality Risk…

    Bristol Myers Squibb (Devens, MA)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director , RBQM - HOCT, ICN will mainly be responsible for ... compliance . **Required Competencies:** + Demonstrated applied knowledge of ICH/ GCP , regulatory guidelines/directives, clinical research processes and principles of… more
    Bristol Myers Squibb (11/28/25)
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  • Associate Clinical Project Management…

    IQVIA (Boston, MA)
    **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate global ... leaders and interfacing with internal and external stakeholders to ensure compliance , quality, and timely delivery of trial milestones. **Key Responsibilities:**… more
    IQVIA (10/22/25)
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  • Director of Research Nursing, Cancer…

    Beth Israel Lahey Health (Boston, MA)
    …and advocating for the health of patients, families, and communities. The Nursing Director for the Cancer Clinical Trials Office (CCTO) reports directly to the CCTO ... Director . The Nursing Director supervises the CCTO...well as establish appropriate quality control procedures to ensure compliance with federal, state, local, and institutional guidelines. Training,… more
    Beth Israel Lahey Health (12/05/25)
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  • Senior Clinical Research Associate - West…

    Parexel (Boston, MA)
    …works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a ... serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH- GCP compliance issues to Local Management and/or Clinical Quality Management… more
    Parexel (12/03/25)
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