Clinical Research Associate II, Late Phase Studies
ICON · Frankfurt, Germany
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Research Associate II role involves managing late-phase clinical trials in Frankfurt, including site qualification, monitoring, and close-out activities. Responsibilities encompass protocol compliance, data quality assurance, and cross-functional collaboration with investigators. Candidates require a scientific degree, two years of CRA experience, knowledge of ICH-GCP guidelines, and fluency in English and German, with approximately 60% travel.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of clinical research associate experience
- Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- English and German language proficiency
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced settings
- Willingness to travel approximately 60% of the time
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff to support study conduct
- Review data and resolve queries to maintain high-quality clinical data
- Prepare and review study documentation including protocols and clinical study reports
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.