JOB DETAILS

Clinical Research Coord (Temple Health-Main Campus)

CompanyTemple University Health System
LocationPhiladelphia
Work ModeOn Site
PostedJuly 29, 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
This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. Coordinates and facilitates the conduct of clinical research protocols, which includes the collection and handling of research specimens, documentation and shipment following IATA guidelines. 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. Coordinates data management for satellite location. 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. IATA Certification class will be provided within 3 months from date of hire.

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 experience in a healthcare setting preferably oncology or clinical trials Required
2 years experience with oncology clinical trials Preferred
1 year experience performing phlebotomy and specimen processing Preferred
General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred

Licenses
Cert Clin Research Coordinator Preferred
Cert Clin Research Prof Preferred
Cert Clin Research Associate Preferred
Key Skills
Clinical researchProtocol complianceData managementSpecimen collectionPhlebotomySpecimen processingOncologyClinical trialsPatient safetyData qualityIATA guidelinesChemotherapy knowledgeRadiation therapy knowledgeParticipant recruitment
Categories
HealthcareScience & Research
Job Information
📋Core Responsibilities
Coordinates and facilitates clinical research protocols, including specimen collection, handling, and shipment according to IATA guidelines. Ensures protocol compliance, participant safety, data quality, and effective recruitment for clinical trials.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
5807
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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