Clinical Research Coordinator

What you’d do

Coordinate 2–6 clinical trials at an on-site Las Vegas research site, from patient recruitment and informed consent to regulatory documentation and site audits. Perform clinical procedures such as vital signs, phlebotomy, ECGs, and lab specimen processing. Full time, fully on-site. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 1–3 years clinical research experience at a clinical investigative site
• Experience working with study participants
• Phlebotomy
• ECG and vital signs
• Fully on-site in Las Vegas, NV