CLINICAL RESEARCH MONITOR

Temple University Health SystemPhiladelphia, PA

About The Position

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).

Requirements

  • Bachelor's Degree Science or other health care discipline Required
  • Combination of relevant education and experience may be considered in lieu of degree Required

Nice To Haves

  • 2 years experience in clinical research monitoring/auditing Preferred
  • 2 years experience in oncology Preferred
  • 2 years experience working in clinical research Preferred
  • Clinical Research Coordinator Certification Preferred
  • Clinical Research Associate Certification Preferred
  • Clinical Research Professional Certification Preferred

Responsibilities

  • 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.
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