Full employer posting
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
Full-Time · Day Shift · 40 hours per week
About the role
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.