JOB DETAILS
CLINICAL RESEARCH COORD
CompanyTemple University Health System
LocationPhiladelphia
Work ModeOn Site
PostedApril 20, 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
Coordinates and facilitates the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provides leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. The position will work closely with the members of the clinical research team to develop effective tools for close monitoring and reporting of trials accrual, and coordinate the timely study activation and submission of protocol amendments.
This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.
Flexibility in work schedule, when possible, must be maintained to ensure coverage of study responsibilities.
Education
Bachelor's Degree Required
Graduate Level Classes or Degree in a relevant program Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years direct experience in a healthcare setting preferably oncology or clinical trials or a minimum of 3 Years related experience Required
General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred
General Experience Previous experience performing phlebotomy and specimen processing Preferred
Licenses
Cert Clin Research Coordinator Preferred or
Cert Clin Research Prof Preferred or
Assn Clin Res Prof - Cert Prof Preferred
This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.
Flexibility in work schedule, when possible, must be maintained to ensure coverage of study responsibilities.
Education
Bachelor's Degree Required
Graduate Level Classes or Degree in a relevant program Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years direct experience in a healthcare setting preferably oncology or clinical trials or a minimum of 3 Years related experience Required
General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred
General Experience Previous experience performing phlebotomy and specimen processing Preferred
Licenses
Cert Clin Research Coordinator Preferred or
Cert Clin Research Prof Preferred or
Assn Clin Res Prof - Cert Prof Preferred
Key Skills
Clinical research coordinationProtocol complianceParticipant recruitmentData quality managementStudy activationProtocol amendmentsOncologyClinical trialsPhlebotomySpecimen processingChemotherapy administrationRadiation therapy administrationRegulatory reporting
Categories
HealthcareScience & ResearchAdministrative
Job Information
📋Core Responsibilities
Coordinates and facilitates clinical research protocols to ensure participant safety, protocol compliance, and high data quality. Collaborates with the clinical research team to manage trial accrual, study activation, and the submission of protocol amendments.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
5675
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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