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    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.
    • Organizational and analytical and problem solving skills.
    • Demonstrated verbal and written skills at professional level.

    CERTIFICATIONS/LICENSURES REQUIRED:

    • SOCRA or ACRP and IATA certification preferred.
    Additional Information


    • Organization: Henry Ford Medical Group
    • Department: Cancer Clinical & Trans Resear
    • Shift: Day Job
    • Union Code: Not Applicable


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