Sr. Clinical Research Associate
ICON · Milan, Italy
The apply link worked recently (not employer-confirmed).
Role summary
This role oversees clinical trial operations across multiple sites in Milan, ensuring compliance with study protocols, regulatory standards, and Good Clinical Practice guidelines. The Senior CRA will monitor site performance, coordinate data collection, and provide training to staff while managing stakeholder relationships. The position requires an advanced degree in life sciences or a 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, medicine, or related field
- Extensive clinical research associate experience with clinical trial process knowledge
- Ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Proficiency with clinical trial software and relevant tools
- Strong communication and stakeholder management capabilities
- Valid driver's license and willingness to travel 60% domestically and internationally
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Coordinate with cross-functional teams on timely and accurate data collection and reporting
- Train site staff and other CRAs on clinical trial conduct standards and best practices
- Maintain relationships with site personnel and stakeholders to facilitate 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.