Clinical Research Monitor II

Temple University Health System • Philadelphia, PA

5d

About The Position

The OCR Clinical Research Monitor II completes, revises, and reviews the requirements necessary to attain and maintain 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 certifications, related training, or education programs may be considered in lieu of those listed below (i.e., Regulatory Affairs).

Requirements

• Bachelor's Degree in Science or other health care discipline
• 2 years experience in oncology
• 2 years experience working as a Clinical Research Monitor
• Certified Clinical Research Associate
• Certified Clinical Research Coordinator
• Certified Clinical Research Professional

Nice To Haves

• Master's Degree in Clinical Research or other applicable science or healthcare discipline
• 3 years experience in oncology clinical research
• Combination of relevant education and experience may be considered in lieu of degree

Responsibilities

• Completes, revises, and reviews requirements for FDA and other regulatory body compliance for clinical trial research.
• Monitors extramural research program investigator-initiated studies at FCCC and other academic institutions.
• Ensures protocol compliance at clinical research sites.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level