Clinical Trial Research Monitor II

he 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. Other applicable certification, related training, or education programs may be considered in lieu of those listed below (i.e. Regulatory Affairs).

he 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).

This role is located in Philadelphia, PA and no traveling is required.

Education
Bachelor's Degree Science or other health care discipline Required
Master's Degree Clinical Research or other applicable science or healthcare discipline Preferred or
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 or
Cert Clin Research Coordinator Required
Cert Clin Research Prof Required

Required Skills


Required Experience