Senior Clinical Research Associate
ICON · US
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
This home-based position involves conducting clinical trial site visits, monitoring protocol compliance, and ensuring data quality across multiple study locations. The role requires a bachelor's degree in a science or health field plus 1–3 years of independent monitoring experience, depending on the level, along with strong knowledge of ICH-GCP guidelines and willingness to travel 60% of the time.
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.