Senior CRA
ICON · Athens, Greece
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Role summary
A world-leading clinical research organization seeks a Senior Clinical Research Associate based in Athens to oversee trial site monitoring and ensure protocol adherence, regulatory compliance, and data integrity. The role involves conducting site visits, collaborating across teams, and mentoring staff, requiring an advanced degree in life sciences or related field, 2–3 years of oncology monitoring experience, and willingness to travel 60% internationally.
What they're looking for
- Advanced degree in life sciences, nursing, or medicine
- Extensive clinical research associate experience with strong trial process knowledge
- 2-3 years monitoring oncology trials
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software
- Excellent communication and stakeholder management abilities
- Valid driver's license and willingness 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 provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection
- Train site staff and other CRAs on clinical trial conduct standards
- Build and maintain effective relationships with site personnel and stakeholders
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.