Clinical Research Trial Monitor

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).

Education
Bachelors Degree: Science or other health care discipline (Required)
Combination of relevant education and experience may be considered in lieu of degree.

Experience
2 Years experience in clinical research monitoring/auditing (Preferred)
2 Years experience in oncology (Preferred)
2 Years experience working in clinical research (Preferred)

License/Certifications
CCRC - Cert Clin Research Coordinator (Preferred) or CCRA - Cert Clin Research Associate (Preferred)
CCRP - Cert Clin Research Prof (Preferred)