• Clinical Research Manager

    ManpowerGroup (Merrimack, NH)
    …within the medical device industry. + Familiarity with GCP, ISO 14155, and clinical trial regulatory processes. + Strong organizational skills, attention to ... to work independently in a fully remote setting. + Experience with clinical trial documentation and regulatory requirements; familiarity with monitoring and… more
    ManpowerGroup (10/30/25)
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  • Financial Analyst - Clinical Trials Office

    Vanderbilt University Medical Center (Nashville, TN)
    …reconciliations with sponsors and complete internal financial close-outs for non-federally funded clinical trial . * Monitor and maintain work tag status (active, ... the MyWorkday, iLab, OnCore, and eSMART systems for non-federally funded clinical trial TECHNICAL CAPABILITIES * Project Management (Intermediate): Planning,… more
    Vanderbilt University Medical Center (10/16/25)
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  • Senior Clinical Research Associate

    ICON Clinical Research (Blue Bell, PA)
    …CRA II consideration and 3 years for Senior CRA. + Strong knowledge of clinical trial processes, regulatory requirements, and ICH-GCP guidelines, with a genuine ... Senior CRA-US-Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving… more
    ICON Clinical Research (10/16/25)
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  • Clinical Research Coordinator

    System One (Ozark, MO)
    …billing of research study visits, and fosters team building to support high-quality clinical trial execution. The CRC is responsible for mentoring staff, ... to detail and ability to manage multiple priorities. + Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) platforms. +… more
    System One (10/09/25)
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  • Sr Director, Project Management,…

    ThermoFisher Scientific (Greenville, NC)
    clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... broad understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; expert… more
    ThermoFisher Scientific (09/03/25)
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  • Clinical Research Contract Specialist II

    Actalent (Orlando, FL)
    …Overview: The Research Contract Specialist is responsible for managing and negotiating clinical trial agreements and related research contracts to ensure ... + Draft, review, and negotiate research-related contracts and amendments, including clinical trial agreements. + Interpret and apply contract terms,… more
    Actalent (11/22/25)
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  • Associate Director, Neuroscience, Clinical

    Bristol Myers Squibb (Princeton, NJ)
    …oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial /biomarkers and asset development as well as ... late-stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written… more
    Bristol Myers Squibb (11/22/25)
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  • Research Coordinator I - Cancer, Clinical

    Houston Methodist (Houston, TX)
    …Source Documents, Case Report Forms, Electronic Data Capture portals and Clinical Trial Management System following established procedures. **QUALITY/SAFETY ... study and regulatory documents. + Under the direction of Research Nurse/ Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or… more
    Houston Methodist (11/13/25)
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  • Research Administrator II ( Clinical

    Beth Israel Lahey Health (Boston, MA)
    …Research awards including federal grants and subcontracts, foundation grants and clinical trial agreements. Pre-award responsibilities require supporting the ... and post award management in an academic research/hospital environment. + Clinical trial and related clinical research experience preferred + Demonstrated… more
    Beth Israel Lahey Health (10/31/25)
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  • Bilingual Part-Time Clinical Research…

    Actalent (Tomball, TX)
    …(CRC) with experience in clinical research to support an ongoing Vaccine clinical trial . The ideal candidate will be able to work independently and ... Job Title: Bilingual Part-Time Clinical Research Coordinator Duration: Open-ended contract (average duration 3-6 months) Job Type: 20 hours per week (Monday, Tuesday… more
    Actalent (11/26/25)
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