Clinical Trial Research Monitor II

Temple Health • Philadelphia, PA

8d • Onsite

About The Position

The OCR Clinical Research Monitor II completes, revises, and reviews requirements needed to attain and maintain compliance with the FDA and other regulatory bodies for clinical trial research, including documentation and processes. The role monitors all extramural research program investigator-initiated studies conducted at FCCC and other academic institutions and ensures protocol compliance at clinical research sites. Other applicable certification, related training, or education programs may be considered in place of those listed, such as Regulatory Affairs. The position is located in Philadelphia, Pennsylvania, and does not require travel.

Requirements

• Bachelor's degree in science or another healthcare discipline, or a combination of relevant education and experience in lieu of a degree.
• At least 2 years of experience in oncology.
• At least 2 years of experience working as a Clinical Research Monitor.
• Certification as a Clinical Research Associate, Clinical Research Coordinator, or Clinical Research Professional.
• Other applicable certification, related training, or education programs may be considered in lieu of the listed qualifications.

Nice To Haves

• Master's degree in Clinical Research or another applicable science or healthcare discipline.
• At least 3 years of experience in oncology clinical research.

Responsibilities

• Complete, revise, and review requirements for attaining and maintaining FDA and other regulatory-body compliance in clinical trial research.
• Monitor extramural research program investigator-initiated studies conducted at FCCC and other academic institutions.
• Ensure protocol compliance at clinical research sites.

What This Job Offers

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