Clinical Research Coordinator II - Cancer Center

What you’d do

Recruit, screen, enroll and consent study participants, coordinate research protocols and appointments, and collect and analyze data. Ensure IRB and regulatory compliance and prepare IRB documents. 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, mathematics
• Documentation and records management
• Data utilization and critical thinking
• IRB and regulatory compliance