Clinical Research Coordinator II - OBGYN

What you’d do

Coordinate OBGYN research protocols: recruit and consent participants, schedule study appointments, collect and analyze data, and prepare IRB documents and reports. Full-time role working with study investigators and other departments. 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 skills
• Experience may substitute for education