Clinical Research COORD

OCR Clinical Research MonitorThe 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).EducationBachelor's Degree Science or other health care discipline Required or Combination of relevant education and experience may be considered in lieu of degree RequiredExperience2 years experience in clinical research monitoring/auditing Preferred2 years experience in oncology Preferred2 years experience working in clinical research PreferredLicensesCert Clin Research Coordinator Preferred or Cert Clin Research Associate Preferred Cert Clin Research Prof Preferred