• Clinical Trial Manager

    ICON Clinical Research (Boston, MA)
    As a CLinical Trial Manager you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... data review and verification activities to ensure accuracy and consistency of clinical trial data. + Nurtures and maintains relationships within the Clinical more
    ICON Clinical Research (06/11/25)
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  • Senior Director, Clinical Trial

    Takeda Pharmaceuticals (Boston, MA)
    …company to inspire you and empower you to shine? Join us as a Senior Director, Clinical Trial Configuration based in Cambridge , MA reporting to the VP, ... to ensure regulatory submission compliance. + Ensures that technologies used in clinical trial (s) (eg, EDCs, eCOA, eConsent, Telehealth, IRT, devices, EDCs… more
    Takeda Pharmaceuticals (05/03/25)
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  • Senior Manager , Clinical Partner…

    Takeda Pharmaceuticals (Boston, MA)
    …procurement, contract management, or supplier relationship management + Strong knowledge of clinical trial processes and regulatory requirements + Experience in ... and commercial constructs + Sound understanding of GCP, ICH guidelines, and clinical trial regulations + Strong strategic thinking and project management… more
    Takeda Pharmaceuticals (06/09/25)
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  • Senior Manager , Programming

    Takeda Pharmaceuticals (Boston, MA)
    …apply advanced knowledge of CDISC standards (SDTM and ADaM), medical terminology, clinical trial methodologies to ensure the compliance with regulatory agencies ... Americas, Inc. for the following job opportunity: **JOB LOCATION:** Cambridge , MA **POSITION** : Senior Manager , Programming...documents and ensure they meet the study requirements; analyze clinical trial data by creating Tables, Listings… more
    Takeda Pharmaceuticals (04/05/25)
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  • Manager , Global Trade Compliance

    Takeda Pharmaceuticals (Boston, MA)
    …of export and import compliance policies and procedures for the organization regarding Clinical Trial Material (CTM) and raw material shipments. + Manage daily ... Ensure adherence to country specific standard operating procedures for importing/exporting clinical trial material and raw materials, including logistics,… more
    Takeda Pharmaceuticals (06/08/25)
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  • Manager , Global Regulatory Affairs,…

    Takeda Pharmaceuticals (Boston, MA)
    …Provide strategic and tactical guidance to teams, including regulatory review of clinical trial documents and collaborates cross functionally to ensure the ... Development Center Ameriacs, Inc. for the following job opportunity: **JOB LOCATION:** Cambridge , MA **POSITION** : Manager , Global Regulatory Affairs, Marketed… more
    Takeda Pharmaceuticals (05/23/25)
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  • Executive Director, Global Program Leader (GPL)

    Takeda Pharmaceuticals (Boston, MA)
    …Join us as an Executive Director, Global Program Leader (GPL) in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our ... in enterprise-wide initiatives to improve speed/cost to market (eg innovative trial designs, improving governance processes, asset strategy etc.) GPLs must +… more
    Takeda Pharmaceuticals (04/12/25)
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