Clinical Research Coordinator, On-Site, Kansas City MO

What you’d do

Coordinate multiple clinical trials including patient recruitment, informed consent, regulatory documentation, and site audits. Perform clinical procedures like vital signs, phlebotomy, ECGs, and lab specimen processing in a full-time role in Kansas City, MO. Found on the employer's careers page on Oct 23, 2026. Apply through the link.

You’ll need

• 1-3 years clinical research experience at investigative site
• Experience managing multiple clinical trials
• Skills in phlebotomy, ECG, vital signs measurement
• Knowledge of site operations and drug development process
• Full-time schedule