Senior clinical Research Associate
ICON · Frankfurt, Germany
The apply link worked recently (not employer-confirmed).
Role summary
This senior-level position involves overseeing clinical trial monitoring across multiple sites to ensure protocol adherence, regulatory compliance, and data integrity. The role requires extensive CRA experience, particularly in oncology and Phase I trials, along with proficiency in GCP standards, site management, and clinical trial software. Candidates must hold a relevant scientific degree, be fluent in German and English, and be prepared to travel approximately 60% of the time.
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
- Oncology and Phase I trial experience
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software
- Fluent in German and English languages
- Willingness to travel approximately 60% of the time
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 data collection and reporting
- Train site staff and other CRAs on clinical trial conduct standards
- Build relationships with site personnel and stakeholders to facilitate 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.