Senior CRA
ICON · Budapest, Hungary
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Senior Clinical Research Associate position overseeing clinical trial monitoring and site management for a large contract research organization. The role requires extensive CRA experience, strong regulatory knowledge, and ability to lead and mentor team members 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 solid understanding of trial processes and regulations
- Proven ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management with clinical trial software proficiency
- Excellent communication and stakeholder management skills to drive compliance
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites to ensure protocol adherence, regulatory compliance, and GCP standard maintenance
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and guide site staff and junior CRAs to maintain high standards of trial conduct
- Build relationships with site personnel and stakeholders to facilitate successful 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.