Clinical Research Coordinator I - Department of Medicine

What you’d do

Recruit, screen, enroll and consent study participants, coordinate research protocols and appointments, and collect and report program data. Ensure IRB and regulatory compliance and help prepare 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 critical thinking
• Writing skills