Clinical Study Coordinator - Detroit, United States - Henry Ford Hospital

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    Description

    GENERAL SUMMARY:
    Under minimal supervision, coordinates clinical research projects in compliance with the

    Code of Federal Regulations. Provide technical support to Principal Investigators.

    Analyze protocol specific requirements and implement quality assurance measures to

    ensure physician, patient and clinician compliance. Abstract medical information from

    various sources in the patient medical record. Report adverse events to medical

    monitor, FDA, and all other governing bodies. Coordinate all external audits and

    monitoring visits, and serve as liaison between institution and sponsor. Serve as

    departmental and system-wide resource.


    EDUCATION/EXPERIENCE REQUIRED:

    • Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely
    related field.

    • Two (2) years of relevant experience preferred. Previous coordinator experience
    preferred.


    CERTIFICATIONS/LICENSURES REQUIRED:
    SOCRA or ACRP and IATA certification preferred

    Additional Information


    • Organization: Henry Ford Medical Group