• Associate Director , Product Manager…

    Bristol Myers Squibb (Princeton, NJ)
    …15+ years of demonstrable experience in pharmaceutical industry with proven expertise in clinical trial execution, data acquisition, and analysis reporting on a ... quality, data products, and analytic ready data solutions for GDD Clinical Intelligence ( Trial Simulation & Modeling, Clinical Data Review, Programming and… more
    Bristol Myers Squibb (10/10/25)
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  • Associate Director Clinical…

    GRAIL (Menlo Park, CA)
    …support Grail's partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director , Clinical Compliance will play a key ... and provide compliance advice on SOPs, processes, and protocols for both clinical trial and companion diagnostic activities, ensuring consistency and compliance… more
    GRAIL (09/16/25)
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  • Associate Medical Director…

    ThermoFisher Scientific (Las Vegas, NV)
    …Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is an office-based ... position for a motivated Physician. The Associate Medical Director serves as the physician...in patient medical status, and unblinding requests) during a clinical trial . + Assesses reported adverse events… more
    ThermoFisher Scientific (08/21/25)
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  • Associate Director…

    Actalent (Conshohocken, PA)
    Job Title: Associate Director of Clinical ...database lock processes. + Knowledge of oncology data and clinical trial processes. + Expertise in CRF ... Data Management Job Description As an Associate Director of Clinical Data Management, you will lead and oversee a team within Clinical Data Management,… more
    Actalent (10/10/25)
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  • Associate Director / Director…

    Gilead Sciences, Inc. (Foster City, CA)
    …teamwork, and excellence. Job Description You will typically lead multiple components of clinical trial programs in immunology clinical development. You may ... For the assigned projects, you are accountable for various aspects of ongoing clinical trial program-related activities. These activities include, but are not… more
    Gilead Sciences, Inc. (10/10/25)
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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 ... Breach review board meetings. + Lead complex quality investigations impacting the clinical trial delivery systems. + Provide Quality Leadership for Serious… more
    Takeda Pharmaceuticals (07/16/25)
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  • Associate Director - Clinical…

    Lilly (Indianapolis, IN)
    …days remote - a generous relocation package can be included with offer The ** Associate Director - Submission Data Delivery** role leads all aspects of global ... data archiving, data standards, and submission process. **Responsibilities:** The Associate Director -Submission Data Delivery provides technical leadership and… more
    Lilly (09/23/25)
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  • Associate Director , Strategic…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    The Associate Director , Strategic Sourcing, Clinical Category Lead, will lead the Strategic Sourcing efforts for R&D categories including data management, ... diagnostics, patient platforms, site management and clinical trial support suppliers across all phases...a value-added service to the organization. **Job Description** The Associate Director , Strategic Sourcing, Clinical … more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Associate Director , Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director , Clinical Research Regulatory Job Description Summary With the ... the portfolio of clinical research undertaken within the department/division. The Associate Director for Regulatory Affairs assists the Director in… more
    University of Pennsylvania (10/09/25)
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  • Associate Medical Director /Medical…

    AbbVie (Cambridge, MA)
    …supervision. + Strong desire to collaborate in a cross-functional setting. + Clinical trial experience in the pharmaceutical industry, academia, or equivalent ... is preferred. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of… more
    AbbVie (09/26/25)
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