Clinical Research Monitor
Temple Health•Philadelphia, PA
•Onsite
About The Position
The OCR Clinical Research Monitor completes, revises, and reviews requirements needed to attain and maintain compliance with FDA and other regulatory bodies for clinical trial research, including documentation and processes. The role monitors extramural research program investigator-initiated studies conducted at FCCC and other academic institutions and ensures protocol compliance at clinical research sites. Other applicable certification, such as Regulatory Affairs, may be considered in lieu of the listed certifications. The position is located in Philadelphia, Pennsylvania, and does not require travel.
Requirements
- Bachelor’s degree in science or another health care discipline, or a combination of relevant education and experience in lieu of a degree.
Nice To Haves
- Two years of experience in clinical research monitoring or auditing.
- Two years of experience in oncology.
- Two years of experience working in clinical research.
- Certification as a Clinical Research Coordinator, Clinical Research Associate, or Clinical Research Professional; other applicable certification, such as Regulatory Affairs, may be considered.
Responsibilities
- Complete, revise, and review requirements for attaining and maintaining regulatory 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.
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What This Job Offers
Job Type
Full-time
