Clinical Research Coordinator I - Cancer Center

What you’d do

Recruit, screen, enroll and consent participants for cancer research studies, coordinate protocols and appointments, collect and report program data, and ensure IRB and regulatory compliance. Full time. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

• CITI training within 90 days of hire
• Knowledge of biology, chemistry, and mathematics
• Documentation and records management
• Data utilization and critical thinking
• Writing skills