About this role
Role Overview
- Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures.
- Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits incl. site qualification, site initiation, routine monitoring and site closure visits.
- Evaluate quality and integrity of site practices while escalating quality issues as appropriate.
Requirements
- Bachelor's or Graduate degree in life sciences, nursing or other health related disciplines or a comparable qualification.
- Minimum two years of on-site monitoring research experience as a CRA in the medical device or pharmaceutical industry or with a CRO.
- Fluent (written and spoken) in German.
- Fluent (written and spoken) in English.
Benefits
- Health insurance
- Retirement plans