Clinical Study Coordinator

4 weeks ago


Hamtramck, United States Henry Ford Health System Full time
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

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