Research Study Coordinator I - 40 hrs/wk - Days - Detroit

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.