Onsite Clinical Study Coordinator: Oncology Trials

City of Hope; Duarte (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

City of Hope’s Orange County Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials across stages from First in Human to Phase III. The role involves patient recruitment, consent, trial coordination, data management, and regulatory compliance in a fast-paced clinical setting.

You will work under the Director of Clinical Research, coordinating with investigators and clinical staff to ensure protocol adherence, safety, and timely reporting of

Qualifications

• 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
• IATA within 1 month of employment
• GCP within 1 month of employment
• Human Subjects Protection (HSP) within 1 month of employment
• Basic Life Support (BLS) within 1 month of employment

Responsibilities

• 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.

Education

Bachelor’s degree in Science, Health or related field

Tools

ACRP certification

SOCRA certification

IATA certification

GCP certification

HSP training

BLS certification

Job description

City of Hope’s Orange County Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials across stages from First in Human to Phase III. The role involves patient recruitment, consent, trial coordination, data management, and regulatory compliance in a fast-paced clinical setting.

You will work under the Director of Clinical Research, coordinating with investigators and clinical staff to ensure protocol adherence, safety, and timely reporting of