Oncology Clinical Research Coordinator - Data Integrity

City of Hope; Duarte (CA); On-site; USD 80,000 - 110,000; Full time

Job summary

City of Hope in Duarte, CA is seeking a Clinical Research Coordinator (CRC) to maintain data integrity across oncology studies, manage case report forms, and support regulatory compliance.

You will work with multiple investigators, coordinate site visits, ensure audit-ready documentation in CTMS, and uphold GCP, FDA, NIH, and HIPAA standards. Minimum education is a Bachelor's degree with 2+ years oncology trial experience.

Qualifications

• Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Experience with oncology clinical trials in an academic setting (2+ years).
• Familiarity with IRB requirements and consent processes.

Responsibilities

• Maintain data integrity across assigned studies and complete case report forms accurately.
• Schedule sponsor monitoring visits and ensure data is audit-ready per contract.
• Manage CTMS records and ensure protocol adherence and regulatory compliance.
• Collaborate with investigators and study teams to resolve data queries and monitor study progress.

Skills

GCP

FDA regulations

NIH guidelines

HIPAA regulations

Education

Bachelor's Degree

Tools

CTMS

Job description

City of Hope in Duarte, CA is seeking a Clinical Research Coordinator (CRC) to maintain data integrity across oncology studies, manage case report forms, and support regulatory compliance.

You will work with multiple investigators, coordinate site visits, ensure audit-ready documentation in CTMS, and uphold GCP, FDA, NIH, and HIPAA standards. Minimum education is a Bachelor's degree with 2+ years oncology trial experience.