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Senior CRA (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
- 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
- Profound experience in monitoring
- Knowledge in preparing documents 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
Weitere Qualifikationen: Senior CRA
- 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
- Profound experience in monitoring
- Knowledge in preparing documents 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
Weitere Qualifikationen: Senior CRA
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges