• Clinical Research Coordinator I, Per…

    Cedars-Sinai (Beverly Hills, CA)
    …experience, contribute to meaningful work, and enjoy a flexible schedule. The Clinical Research Coordinator I works independently providing study coordination, ... consent process. Responsible for accurate and timely source documents, data collection, documentation, entry , and reporting including...research needs. **Req ID** : 12856 **Working Title** : Clinical Research Coordinator I, Per Diem -… more
    Cedars-Sinai (10/13/25)
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  • Clinical Research Coordinator II…

    Cedars-Sinai (Los Angeles, CA)
    …**Join our team and contribute to groundbreaking research.** We are seeking a dedicated Clinical Research Coordinator II to join our team. The ideal candidate ... in oncology research are strongly encouraged to apply. The Clinical Research Coordinator II serves as the...informed consent process. + Responsible for accurate and timely data collection, documentation, entry and reporting, including… more
    Cedars-Sinai (09/04/25)
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  • Clinical Research Coordinator 1 (A)

    University of Miami (Miami, FL)
    Coordinator 1 to work on the UHealth campus. The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has ... a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits… more
    University of Miami (08/26/25)
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  • Clinical Research Coordinator I,…

    Cedars-Sinai (Los Angeles, CA)
    **Job Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol ... informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry , and reporting including timely response… more
    Cedars-Sinai (10/13/25)
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  • Clinical Research Coordinator I…

    Cedars-Sinai (CA)
    **Job Description** **Grow your career at Cedars-Sinai!** The Clinical Research Coordinator I works independently providing study coordination, screening of ... consent process. Responsible for accurate and timely source documents, data collection, documentation, entry , and reporting including...the most. **Req ID** : 12453 **Working Title** : Clinical Research Coordinator I - Emergency Medicine… more
    Cedars-Sinai (10/12/25)
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  • Clinical Research Coordinator II

    Actalent (Orlando, FL)
    …+ Work with assistant clinical coordinators to ensure compliant data entry into registries, patient records, and research-specific database systems. ... Clinical Research Coordinator II Job Description...multiple tasks effectively and timely. + Knowledge of HIPAA data protection and patient advocacy, or similar awareness of… more
    Actalent (10/11/25)
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  • Coordinator I - Clinical Research

    HonorHealth (AZ)
    …is responsible for the day-to-day management of project activities and resources and overall clinical data and protocol management for the conduct of clinical ... following activities: recruitment, screening, obtaining informed consent, reviewing source documents, data collection, data entry , query resolution,… more
    HonorHealth (09/12/25)
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  • Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …and storage of biological samples and related study documents, and collection of clinical data . Assist with Institutional Review Board (IRB) filings and ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title...studies, includes; subject recruitment, informed consent, chart maintenance and data entry + Coordinate IRB submissions and… more
    University of Pennsylvania (07/24/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …and storage of biological samples and related study documents, and collection of clinical data . Assist with Institutional Review Board (IRB) filings and ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title...studies, includes; subject recruitment, informed consent, chart maintenance and data entry + Coordinate IRB submissions and… more
    University of Pennsylvania (10/03/25)
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  • Assistant Clinical Research…

    Stanford University (Stanford, CA)
    …potential participants, schedule and interview potential participants, and coordinate collection of clinical data . The ACRC will work under supervision of the ... Assistant Clinical Research Coordinator - Recruitment (1...and tests, score test measurements and questionnaires, and code data for computer entry . Perform quantitative review… more
    Stanford University (09/16/25)
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