CLINICAL RESEARCH MONITOR

About the role

The OCR Clinical Research Monitor is responsible for completing, revising, and reviewing requirements to ensure compliance with FDA and other regulatory bodies for clinical trial research. This includes both a documentation and process level approach.

Responsibilities

• Maintains compliance with FDA and other regulatory bodies for clinical trial research
• Makes sure protocols are followed at clinical research sites
• Monitors extramural research programs being conducted at FCCC and other academic institutions
• Ensures adherence to clinical research standards

Requirements

• Bachelor's Degree in Science or other health care discipline
• 2 years experience in clinical research monitoring/auditing
• Prior experience in oncology preferred
• Prior experience in clinical research preferred

Preferred Qualifications

• Clinical Research Coordinator Certification
• Clinical Research Associate Certification