Offer summary
Qualifications:
College/University degree in Life Sciences, Extensive on-site monitoring experience in phase 2/3 trials, Proficiency in English and German, Experience with complex clinical trials, Ability to travel.
Key responsabilities:
- Perform Pre-Study, Initiation, Interim, and Close-Out monitoring visits
- Ensure site staff has adequate qualifications and resources
- Train investigational site staff as necessary
- Support preparation of regulatory and EC submissions when applicable
- Work in a dynamic team environment