Senior Research Coordinator

What you’d do

Coordinate multiple clinical trials on-site in Lexington, KY, managing patient recruitment, informed consent, regulatory documentation, and site audits. Perform clinical procedures like vital signs, phlebotomy, ECGs, and lab specimen processing during full-time shifts. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• Experience managing multiple clinical trials
• Skills in phlebotomy and ECGs
• Knowledge of site operations and drug development
• Full-time on-site work in Lexington, KY