• Associate Clinical Project…

    IQVIA (Parsippany, NJ)
    **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
    IQVIA (09/25/25)
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  • Associate Clinical Project Manager,…

    IQVIA (Philadelphia, PA)
    …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is accountable for… more
    IQVIA (09/13/25)
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  • Sr. Clinical Research Associate

    ICON Clinical Research (Naperville, IL)
    …a Clinical Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + Proven ability to manage multiple ... Senior Clinical Research Associate ICON plc is...will play a critical role in overseeing and managing clinical trial activities to ensure they are… more
    ICON Clinical Research (09/20/25)
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  • Clinical Research Associate 2

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …set-up, central lab set-up, and other vendor selection processes.** + **Maintaining clinical trial management system (CTMS) information pertaining to the study ... **Knowledge, Skills, and Abilities:** Good knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, and company SOPs. Good… more
    Grifols Shared Services North America, Inc (08/08/25)
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  • Clinical Trials - Clinical Data…

    Lilly (Indianapolis, IN)
    …position 3 days onsite/2 days remote **Purpose:** This role is responsible for trial level clinical data strategy including database structure, content and ... with key study partners to define, implement, and deliver clinical data management packages. This role is responsible for...data management packages. This role is responsible for providing trial leadership and ownership for a particular trial more
    Lilly (09/25/25)
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  • Clinical Research Associate

    Hartford HealthCare (Hartford, CT)
    …is primarily responsible for the overall design, conduct, and management of the clinical trial , the SrCRA leads, facilitates and coordinates all clinical ... *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the...with meeting the goals outlined in the protocol and clinical trial agreement * Motivate others, monitor… more
    Hartford HealthCare (09/06/25)
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  • Associate Specialist, Clinical

    Edwards Lifesciences (Boston, MA)
    …exam results for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters of study hypothesis, ... as well as to monitor clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Verify trial more
    Edwards Lifesciences (09/19/25)
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  • Associate Clinical Lead Director,…

    IQVIA (Durham, NC)
    **Job Overview:** Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and working alongside clinical teams to ... by bringing new drugs to the market faster. The Associate Clinical Lead Director is a member...Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying… more
    IQVIA (09/19/25)
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  • Associate Clinical Site Lead

    Abbott (Minneapolis, MN)
    …fingersticks. Summary Under the supervision of senior colleague/manager (or delegate), the Associate Clinical Site Lead drives study execution and operational ... (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and ...a level that allows for appropriate collaboration with Abbott clinical staff, eg Site CRA, Site Contract Associate more
    Abbott (09/19/25)
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  • Clinical Research Associate ll

    Abbott (Alameda, CA)
    …members, peers, and management. + Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical ... documents required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and Reports). + May interact with RA/QA in responding… more
    Abbott (08/08/25)
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