Senior Clinical Research Associate
ICON · Rome, Italy
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Role summary
A global clinical research organization seeks an experienced Senior Clinical Research Associate for its Rome office. The role involves monitoring trial sites for protocol compliance and GCP adherence, conducting site visits, managing data integrity, and training staff across multiple projects. The position requires an advanced degree in life sciences or related field, extensive CRA experience, and willingness to travel internationally at least 60% of the time.
What they're looking for
- Advanced degree in life sciences, nursing, or medicine
- Extensive clinical research associate experience with clinical trial process knowledge
- Proven ability to manage multiple sites and projects concurrently
- Expertise in monitoring practices, data integrity, and site management
- Strong communication and stakeholder management skills
- Proficiency in clinical trial software and relevant tools
- Valid driver's license and ability to travel 60% internationally and domestically
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, resolve issues, and support trial execution
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train site staff and other CRAs on clinical trial conduct standards and requirements
- Build and maintain relationships with site personnel to ensure smooth trial operations
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.