• Clinical Research Associate

    IQVIA (Durham, NC)
    IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience ... that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...* Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good … more
    IQVIA (07/04/25)
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  • Clinical Research Associate

    Trinity Health (Fort Lauderdale, FL)
    …**Description:** Summary This person will be responsible for the conduct of multiple clinical research activities. Ideal candidate will have industry sponsored ... Person is able to work with minimal supervision and within the scope of clinical research protocols, participates in research activities which may include:… more
    Trinity Health (07/19/25)
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  • Clinical Research Data

    AdventHealth (Orlando, FL)
    …601 EAST ROLLINS STREET, Orlando, 32803 **The role you'll contribute:** The Clinical Research Data Operations Supervisor serves the AdventHealth ... guidelines. The Supervisor is able to function as a Clinical Research Data Coordinator as...field and at least 2 years of experience in clinical research or + Associate 's… more
    AdventHealth (05/19/25)
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  • Clinical Research Data

    University of Southern California (Los Angeles, CA)
    Clinical Research Data Specialist IApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical - ... data from medical records. Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical more
    University of Southern California (07/23/25)
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  • Clinical Research Associate

    Touro University (Hawthorne, NY)
    …adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities ... clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research...clinical team and report as required. + Enter data on Hematology, Oncology and Stem Cell Transplant patients… more
    Touro University (07/24/25)
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  • CRA III ( Associate Clinical

    Abbott (Alameda, CA)
    …and audit Trial Master File to ensure inspection readiness. + Perform review of clinical data listings for completeness and accuracy, and escalate issues to the ... life sciences or equivalent with minimum 7 years of clinical research experience + Must have 4...clinical trial process including study design and conduct; clinical data management systems; clinical more
    Abbott (06/27/25)
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  • Clinical Research Associate

    University of Southern California (San Diego, CA)
    Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Research - Associate ... San Diego, California The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute… more
    University of Southern California (07/15/25)
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  • Clinical Research Associate

    ICON Clinical Research (Orlando, FL)
    As a Clinical Research Associate you...and ensure proper storage, return, or destruction + Resolve data queries and drive timely, high-quality data ... will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What You Will Be Doing:** + Serve… more
    ICON Clinical Research (07/15/25)
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  • (Senior) Clinical Research

    IQVIA (Carlsbad, CA)
    …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
    IQVIA (07/14/25)
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  • CRA I ( Associate I Clinical

    Abbott (Alameda, CA)
    …(TMF) and upload to eTMF to ensure inspection readiness. + Perform review of clinical data listings for completeness and accuracy; and escalate issues to the ... The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle...preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate… more
    Abbott (06/12/25)
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