Clinical Research Coordinator II - Medicine

What you’d do

Recruit, screen, enroll and consent study participants, coordinate research protocols and appointments, and collect and analyze data. Ensures IRB and regulatory compliance and prepares IRB documents. Full time. Found on the employer's careers page on Oct 19, 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 complex problem solving
• IRB and regulatory compliance