CLINICAL STUDY COORD - 10032269

Duarte, CA

City of Hope is an independent biomedical research and treatment center for cancer, diabetes and other life-threatening diseases.

Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope™, a wholly owned subsidiary, was launched in 2019 and is dedicated to serving employers and their health care partners by providing access to City of Hope’s exceptional cancer expertise.

A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is ranked among the nation’s “Best Hospitals” in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Pay Rate: $43.18 - $66.92 per hour

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte

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.

Orange County 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.

Qualifications - External

Your qualifications should include:

Bachelor’s degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.
Minimum of 2 years research or relevant clinical experience
ACRP or SOCRA certification within 1 year of employment
International Air Transport Association (IATA) within 1 month of employment
Good Clinical Practice (GCP) within 1 month of employment
Human Subjects Protection (HSP) within 1 month of employment
Basic Life Support (BLS) within 1 month of employment

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here.

To learn more about our Comprehensive Benefits, please CLICK HERE.

CLINICAL STUDY COORD - 10032269

Duarte, CA

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City of Hope is an independent biomedical research and treatment center for cancer, diabetes and other life-threatening diseases.

Pay Rate: $43.18 - $66.92 per hour

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte

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.

Qualifications - External

Your qualifications should include:

Bachelor’s degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.
Minimum of 2 years research or relevant clinical experience
ACRP or SOCRA certification within 1 year of employment
International Air Transport Association (IATA) within 1 month of employment
Good Clinical Practice (GCP) within 1 month of employment
Human Subjects Protection (HSP) within 1 month of employment
Basic Life Support (BLS) within 1 month of employment

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here.

To learn more about our Comprehensive Benefits, please CLICK HERE.

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