Description
We are looking for a Senior CRA
Senior CRA (m/f)
Referenz: -en
Beginn: asap
Dauer: 12 MM
Ort: in Zurich region
Branche: Herstellung von pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Monitoring of sites
- Check compliance with study protocol, ICH GCP and local regulations
- Ensure ethical conduct of clinical studies
- Write reports within the agreed timeframe
- Conduct feasibility assessment, Pre-study Visits, Sinte Initiation and Close-Out visits
- Review of Investigator Site Files, ensure proper handling of IMP
Ihre Qualifikation
- Profound experience in monitoring
- Knowledge in preparing docuemtns for submissions to IRB/IEC and Swissmedic
- Experience in contract negotiations and know how of local regulations (CH)
- Fluent in French, German and English
- Experience in contract negotiations, excellent knowledge of local regulations, experience in project management
Skills:
- Senior CRA