Senior CRA
ICON · Warsaw, Poland
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position at ICON overseeing clinical trial activities across multiple sites in a sponsor-dedicated model. Responsible for monitoring protocol adherence, ensuring regulatory compliance, and managing data integrity while supporting site teams and cross-functional stakeholders.
What they're looking for
- Advanced degree in life sciences, nursing, medicine, or related field
- Extensive CRA experience with strong knowledge of clinical trial processes and GCP standards
- Demonstrated ability to manage multiple sites and projects with organizational skills
- Expertise in monitoring practices, data integrity, site management, and clinical trial software
- Excellent communication and stakeholder management abilities
- Availability to travel 60% of the time; valid driver's license required
- Legal right to work in Poland
What you'll be doing
- Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on accurate and timely data collection and reporting
- Train site staff and other CRAs on clinical trial conduct and compliance standards
- Build and maintain relationships with site personnel to ensure trial operation effectiveness
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.