Sr. CRA
ICON · Frankfurt, Germany
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate responsible for overseeing clinical trial activities across multiple sites in Frankfurt. The role involves monitoring protocol adherence, conducting site visits, managing data integrity, and mentoring staff while ensuring compliance with regulatory standards and Good Clinical Practice requirements.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Extensive Clinical Research Associate experience with deep knowledge of trial processes and regulations
- Demonstrated ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, site management, and clinical trial software
- Fluent in German and English
- Willingness to travel approximately 60%
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard adherence
- Conduct site visits to assess performance, identify issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and mentor site staff and other CRAs on clinical trial conduct standards
- Build and maintain relationships with site personnel and stakeholders to support 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.