Senior CRA
ICON · Warsaw, Poland +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position overseeing clinical trial monitoring and site management across multiple projects. Requires extensive CRA experience, strong regulatory knowledge, and ability to lead teams while ensuring protocol adherence and data integrity.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with deep knowledge of trial processes and regulations
- Proven ability to manage multiple sites and projects with strong organizational skills
- Expert-level monitoring practices, data integrity expertise, and clinical trial software proficiency
- Excellent communication and stakeholder management with ability to drive compliance
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for adherence to study protocols, regulatory requirements, 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
- Provide training and guidance to site staff and junior CRAs on clinical trial conduct standards
- Build and maintain relationships with site personnel and stakeholders for smooth 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.