JOB DETAILS
Clinical Research Monitor II
CompanyTemple University Health System
LocationPhiladelphia
Work ModeOn Site
PostedJuly 6, 2026
About The Company
At Temple Health, more is how excellence is defined.
Temple Health is a Philadelphia-based academic health system redefining what’s possible in advanced patient care. Through clinical innovation, pioneering research, and world-class education, Temple is transforming complex medical challenges into real-world solutions—delivering more answers, more options, and more possibilities for patients.
Powered by more than 1,700 physicians, researchers and scientists across Temple University Hospital, the Lewis Katz School of Medicine and Fox Chase Cancer Center, Temple accelerates the translation of scientific discovery into practical therapies, united by a shared commitment to advancing medicine and expanding what patients can expect from their care.
Temple’s depth of expertise enables outcomes once thought impossible—more specialized expertise, more innovation, and more opportunities to expect what’s next in medicine.
It Takes Temple Health.
About the Role
The OCR Clinical Research Monitor II, 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, related training, or education programs may be considered in lieu of those listed below (i.e. Regulatory Affairs).
Education
Bachelor's Degree Science or other health care discipline Required
Master's Degree Clinical Research or other applicable science or healthcare discipline Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years experience in oncology Required
2 years experience working as a Clinical Research Monitor Required
3 years experience in oncology clinical research Preferred
Licenses
Cert Clin Research Associate Required or
Cert Clin Research Coordinator Required
Cert Clin Research Prof Required
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, related training, or education programs may be considered in lieu of those listed below (i.e. Regulatory Affairs).
Education
Bachelor's Degree Science or other health care discipline Required
Master's Degree Clinical Research or other applicable science or healthcare discipline Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years experience in oncology Required
2 years experience working as a Clinical Research Monitor Required
3 years experience in oncology clinical research Preferred
Licenses
Cert Clin Research Associate Required or
Cert Clin Research Coordinator Required
Cert Clin Research Prof Required
Key Skills
Clinical Trial MonitoringFDA ComplianceRegulatory AffairsProtocol ComplianceOncology ResearchClinical DocumentationSite Monitoring
Categories
HealthcareScience & Research
Job Information
📋Core Responsibilities
The role involves monitoring extramural research program investigator-initiated studies to ensure protocol compliance. It also requires reviewing and maintaining documentation to meet FDA and other regulatory body requirements.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
5771
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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