Clinical Study Coord

City of Hope • Duarte, CA

3d • Onsite

About The Position

City of Hope’s Orange County Medical Center is seeking 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 coordinates First in Human through Phase III trials and Investigator-Initiated Trials. The role requires knowledge of clinical trial regulations, strong organizational skills, and effective collaboration with investigators and clinical staff in a fast-paced environment.

Requirements

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

Responsibilities

• Understand and apply federal regulations, including FDA, OHRP, GCP/ICH, and HIPAA requirements, as well as institutional policies.
• Follow and execute clinical trial protocols and procedures.
• Coordinate participant recruitment, informed consent, and care.
• Communicate with participants, investigators, and sponsors to support clear understanding and compliance.
• Monitor and document participant eligibility, safety, and protocol adherence.
• Report adverse events promptly.
• Pursue ongoing education and training, stay current with clinical research information, and maintain necessary certifications and licensure.

What This Job Offers

• Job Type: Full-time