Study Delivery Specialist
ICON · Vilnius, Lithuania +2 more
The apply link worked recently (not employer-confirmed).
Role summary
This global project delivery role supports clinical trial operations across multiple countries, managing study lifecycle activities from initiation through closeout. The specialist coordinates with study managers and cross-functional teams to maintain compliance, oversee vendor relationships, track performance metrics, and ensure inspection readiness. Prior experience in global clinical research project delivery is required.
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.