Senior Clinical Research Associate
ICON · Prague, Czechia
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate responsible for overseeing clinical trial monitoring activities across multiple sites in the Czech Republic. The role involves conducting site visits, ensuring protocol and regulatory compliance, directing data collection efforts, and mentoring junior staff. This home-based position requires extensive CRA experience, a scientific degree, and willingness to travel approximately 60%.
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.