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Clinical Study Coordinator- Full time- Clinical Trials

Henry Ford Hospital

This is a Full-time position in Detroit, MI posted May 1, 2021.

* 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.

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