Clinical Study Coordinator

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