Clinical Research Associate - Sponsor Dedicated

What you’d do

Monitor clinical trial sites and manage site relationships to ensure studies follow the protocol, regulations, and sponsor requirements, including reviewing reported study data. Full time role based in Overland Park, KS. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Bachelor's in scientific discipline or health care preferred
• CRA training program or prior monitoring experience may be required
• Site monitoring and management skills
• Knowledge of study protocols and regulations