Job Details

OCR Clinical Research Monitor II

The OCR Clinical Research Monitor II 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, related training, or education programs may be considered in lieu of those listed below (i.e. Regulatory Affairs).

Education

Bachelor's Degree Science or other health care discipline Required

Master's Degree Clinical Research or other applicable science or healthcare discipline Preferred

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

Experience

2 years experience in oncology Required

2 years experience working as a Clinical Research Monitor Required

3 years experience in oncology clinical research Preferred

Licenses

Cert Clin Research Associate Required

Cert Clin Research Coordinator Required

Cert Clin Research Prof Required