• Clinical Research Associate 3

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …IVRS 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:** Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, and company SOPs.… more
    Grifols Shared Services North America, Inc (11/08/25)
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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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  • Senior Clinical Research Associate

    ThermoFisher Scientific (Suwanee, GA)
    clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... required. Ensures study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC check of reports generated from… more
    ThermoFisher Scientific (11/26/25)
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  • Study Associate I, Clinical

    Taiho Oncology (Princeton, NJ)
    …sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical, ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
    Taiho Oncology (11/13/25)
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  • Clinical Research Associate II/Sr.…

    Parexel (Atlanta, GA)
    …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... Midwest, West Coast, Northeast & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
    Parexel (11/22/25)
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  • Clinical Employee Rotational Program (CERP)…

    Lilly (Indianapolis, IN)
    …research. Your work or project may include but are not limited to the following: + Clinical Trial Planning and Design + Clinical Trial Investigator ... Communication and Documentation + Clinical Supply and Delivery + Clinical Trial Budgeting and Financial Management + Clinical Research Training and… more
    Lilly (10/18/25)
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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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  • 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 (11/22/25)
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  • Principal Clinical Research…

    Boehringer Ingelheim (Athens, GA)
    **Description** The Principal Clinical Research Associate will manage a team of Clinical Research Associates (CRA) that assist the Clinical Scientists ... and line managers in execution and control of Clinical GI internal and external laboratory studies and field...conducts on-site and in-house monitoring to verify that reported study/ trial data are accurate, complete, and verifiable from source… more
    Boehringer Ingelheim (11/18/25)
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  • Associate Director, Digital Clinical

    BeOne Medicines (San Mateo, CA)
    …responsible to enhance Global Clinical Operations' productivity and reduce clinical trial inefficiencies, by detailing the business critical capabilities ... **General Description:** The ** Associate Director** **,** **Digital Clinical Operations**...to Study Close Out with focus on use of Clinical Trial Management System (CTMS) application. This… more
    BeOne Medicines (11/18/25)
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