Clinical Research Monitor

The OCR Clinical Research Monitor, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level.

Monitors all extramural research program investigator initiated studies being conducted at FCCC and other academic institutions. Ensures protocol compliance at the clinical research sites. Other applicable certification may be considered in lieu of those listed below (i.e. Regulatory Affairs).

Education

Bachelor's Degree Science or other health care discipline Required or

Combination of relevant education and experience may be considered in lieu of degree Required

Experience

2 years experience in clinical research monitoring/auditing Preferred

2 years experience in oncology Preferred

2 years experience working in clinical research Preferred

Licenses

Cert Clin Research Coordinator Preferred or

Cert Clin Research Associate Preferred

Cert Clin Research Prof Preferred '405750