• Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations ... program. This position will require line management responsibility of Directors, Associate Directors, Clinical Study Managers, who are primarily responsibility… more
    HireLifeScience (08/23/25)
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  • Merck & Co. (Rahway, NJ)
    Job Description Role Summary The Associate Director of Procurement for Capital Projects will be responsible for overseeing and managing procurement activities ... of Capital Procurement Project Execution within the Global Capital Procurement organization, the Associate Director will serve as the primary point of contact… more
    HireLifeScience (09/30/25)
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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 (07/25/25)
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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. **This role is located in Cambridge, MA and is Hybrid (not… more
    Takeda Pharmaceuticals (07/16/25)
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  • Associate Director , Neuroscience,…

    Bristol Myers Squibb (Cambridge, MA)
    …Operations and Procurement. + Determines appropriate assays and vendors for clinical biomarkers, and manages outsourcing of biomarker assay development ... of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and… more
    Bristol Myers Squibb (10/01/25)
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  • Associate Director WFM Capacity…

    CenterWell (Columbia, SC)
    …expansion, vendor allocation, outsourcing , and automation. Additionally, the Associate Director collaborates with Real-Time Management, Scheduling, and ... caring community and help us put health first** The Associate Director of WFM Capacity Planning is...chronic and complex illnesses, as well as offer personalized clinical and educational services to improve health outcomes and… more
    CenterWell (10/01/25)
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  • Associate Director , Global R&D…

    BeOne Medicines (Emeryville, CA)
    **General Description:** This position will be responsible for the management of clinical outsourcing needs in support of BeOne's current and planned clinical ... metrics, and vendor oversight/governance. This position will also be responsible for clinical study budget estimation and budget management during the study life… more
    BeOne Medicines (08/27/25)
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  • Associate Director , WW Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …Patients, and Payers in accordance with local regulations. **Key Responsibilities:** The Associate Director of Medical Communications is accountable for the ... personal lives. Read more: careers.bms.com/working-with-us . Position reports to the Executive Director (or Director ) of Medical Communications within WW Medical… more
    Bristol Myers Squibb (09/10/25)
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  • Associate Director , Biostatistics

    Pfizer (Collegeville, PA)
    …you will: + Provide scientifically rigorous statistical input into clinical development plans, protocol development, statistical analysis plans, regulatory ... resource allocation and progress monitoring. + Develop effective collaborations with clinical teams and partner lines (eg, Development Operations, Safety Risk… more
    Pfizer (10/01/25)
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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 (08/08/25)
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