Clinical/Translational Research Coordinator II

What you’d do

Coordinates approval processes and conduct of clinical and translational research protocols, preparing and processing IRB proposals, amendments, continuing reviews and adverse event reports, and maintaining regulatory documents for sponsor and authority site visits. Full time. Found on the employer's careers page on Oct 20, 2026. Apply through the link.

You’ll need

• IRB proposal preparation and submission
• Regulatory document maintenance
• Knowledge of federal research regulations
• Support of sponsor and regulatory site visits