Senior Clinical Research Associate
ICON · Los Angeles, CA +4 more
The apply link worked recently (not employer-confirmed).
Role summary
This position involves serving as the primary liaison between oncology investigational sites and sponsors across the West region. Responsibilities include conducting site visits, ensuring regulatory compliance, managing documentation systems, monitoring patient safety, and coordinating drug accountability. Requires a Bachelor's degree in Life Sciences or RN credential, 3+ years of on-site monitoring experience in pharmaceutical/CRO settings, and willingness to travel up to 50% regionally.
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.