• Assistant Clinical Research

    Stanford University (Stanford, CA)
    Assistant Clinical Research Coordinator **School of Medicine, Stanford, California, United States** Research Post Date Jul 14, 2025 Requisition # 106838 ... Stanford University is seeking anAssistant Clinical Research Coordinator to perform administrative support...and thank you letters to subjects upon completion of trial activities. Assist with post- study activities, as… more
    Stanford University (08/07/25)
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  • Assistant Clinical Research

    UCLA Health (Los Angeles, CA)
    Research Coordinator in contributing to the overall operational management of clinical research / trial / study activities. In this role, you will ... Description The Assistant Clinical Research Coordinator assists the ...and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations. Salary offers are determined… more
    UCLA Health (09/04/25)
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  • Clinical Research Associate, Sponsor…

    IQVIA (Carlsbad, CA)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...* Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good… more
    IQVIA (08/13/25)
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  • Sr. Scientist Clinical Research

    Abbott (Santa Clara, CA)
    …directed by your manager. **What You'll Work On** + Writes clinical trial protocols, protocol amendments, clinical study reports, and scientific ... in more than 160 countries. **Job Title** **Sr. Scientist Clinical Research ** **About Abbott** Abbott is a...bodies about submissions. + Participates in the development of clinical strategy and trial design by conducting… more
    Abbott (06/21/25)
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  • Clinical Research Coordinator

    Actalent (Pasadena, CA)
    …an experienced Clinical Research Coordinator to manage multiple clinical trials , ensure protocol compliance, and support patient engagement throughout ... study lifecycle. Key Responsibilities: + Manage 6-8 clinical trials + Conduct patient screening, informed...+ RN/LVN or Bachelor's degree + 5+ years of clinical research experience + Knowledge of FDA,… more
    Actalent (09/04/25)
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  • Clinical Research Coordinator

    Actalent (San Diego, CA)
    …experience and a Bachelor's degree in related area + Demonstrated experience in clinical trials research . Strong knowledge of experimental protocols, data ... develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as...regulatory guidelines. Oversee the quality of the medical and clinical research data. Provide direction and guidance… more
    Actalent (09/06/25)
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  • EDC/ Clinical Devices Research

    US Tech Solutions (South San Francisco, CA)
    …Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining device ... Research Coordinator, under the oversight of the Clinical Trial Manager and PI, is responsible... Manager and PI, is responsible for independently conducting clinical research sessions with study more
    US Tech Solutions (07/18/25)
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  • Clinical Research Nurse

    Actalent (Santa Maria, CA)
    …to plan, coordinate, implement, and complete clinical trials and research projects. You will oversee complex studies in cardiology, provide direct ... for research nursing excellence. Key Responsibilities + Oversee and manage research studies focused on complex medical conditions, particularly in Oncology.… more
    Actalent (09/03/25)
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  • CRA II

    ICON Clinical Research (Long Beach, CA)
    …Coast or Central US ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ... clinical development. We are currently seeking a Clinical Research Associate II to join our...will play a pivotal role in designing and analyzing clinical trials , interpreting complex medical data, and… more
    ICON Clinical Research (08/22/25)
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  • Clinical Research Nurse

    Parexel (Glendale, CA)
    …in medical records and progress notes. Update and maintain the contents of the Clinical Study File. + Perform or arrange for phlebotomy, urine collection, sample ... participants. Contributes to the development and implementation of study / research objectives. + Assess, monitor, record, and...+ Act as participant advocate in the conduct of clinical studies . **Qualifications** + At least 2… more
    Parexel (07/31/25)
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