Clinical Research Coordinator II

What you’d do

Recruit, screen, enroll and consent participants across primary care and specialty clinics, coordinate research protocols and appointments, collect and report program data, and handle IRB submissions and 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, mathematics and records management
• Data utilization and complex problem solving
• IRB and regulatory compliance
• Writing skills