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City of Hope
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$135,054 / year median in California
+16% projected growth
Job Description
Learn More City of Hope $44.90 - $69.60 / hr United States, California, Duarte 1500 East Duarte Road (Show on map) Jul 20, 2026 Clinical Study Coordinator - Clinical Research (On-Site) Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. Duarte Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations, strong organizational skills, and the ability to collaborate with investigators and clinical staff in a fast-paced environment. As a successful candidate, you will: Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
Follow and execute clinical trial protocols and procedures.
Coordinate participant recruitment, informed consent, and care.
Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.
Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.