Senior Clinical Research Associate
ICON · Blue Bell +5 more
The apply link worked recently (not employer-confirmed).
Role summary
This Senior Clinical Research Associate role involves managing clinical trial sites across phases II–IV, with responsibilities including site selection, initiation, closeout, regulatory submissions, and protocol oversight. The position requires 18+ months of CRA monitoring experience, a science or medical degree, fluency in German and English, and 60% travel availability. The sponsor-dedicated focus is on dermatology and rare disease trials.
What they're looking for
- 18+ months clinical research associate monitoring experience in phase I-III trials
- College degree in medicine, science, or equivalent field
- Medium-sized study experience including startup and closeout activities
- ICH-GCP guideline knowledge and medical data evaluation capability
- Fluent written and verbal communication in German and English
- Valid driving license and availability for 60% travel
- Ability to meet tight deadlines independently
What you'll be doing
- Establish and monitor investigational sites for dermatology and rare disease trials phases II-IV
- Submit regulatory documents and prepare ethics/IRB approval submissions
- Manage sponsor queries and maintain study documentation
- Monitor study cost efficiency and prepare feasibility assessments
- Mentor and train junior clinical research associates as needed
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.