Full employer posting
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). This role is located in Philadelphia, PA and no traveling is required.
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
Full-Time · Day Shift · 40 hours per week
About the role
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.