CRA II
ICON · Warsaw, Poland
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Research Associate II position at ICON involves monitoring clinical trial sites through in-person and remote visits, verifying data quality, and ensuring protocol compliance. Responsibilities include site management activities, training delivery, system reviews, and ongoing stakeholder communication. The role requires at least 2 years of CRA experience, familiarity with clinical trial processes, and knowledge of relevant software platforms, with 50% travel expected.
What they're looking for
- Bachelor's degree in health-related or life science field or equivalent
- Minimum 2 years of experience as CRA
- Understanding of drug development and clinical trial execution processes
- Experience with site monitoring and risk-based monitoring delivery
- Knowledge of Veeva EDC, TMF, and CTMS systems
What you'll be doing
- Conduct site visits onsite and remotely to assess suitability and study conduct
- Review site records for protocol compliance, data quality, and participant safety
- Develop communications and monitoring documentation with study sites
- Deliver and document study training to site personnel
- Support sites with compliance issues and escalate problems as needed
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.