Clinical Research Associate
ICON · Long Beach, CA +7 more
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Role summary
This Clinical Research Associate II role involves monitoring early-stage clinical trials across multiple western U.S. states, with responsibilities including site qualification, protocol compliance verification, data integrity oversight, and study documentation review. The position requires a bachelor's degree in a scientific or healthcare field, minimum two years CRA experience with at least two years in Phase I trials, strong knowledge of ICH-GCP guidelines, and willingness to travel 65-75% within the west region.
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.