Description
We are looking for a
Clinical Trial Documentation Specialist (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Place: in Basel region
Branch: Herstellung von pharmazeutischen Erzeugnissen
Your tasks:
- Keep TMFs audit ready
- Set-up, maintain and archive of TMF and eTMF
- Perform quality checks of TMFs within specific timelines
Your qualifications
- Education within the Life Sciences industry
- Experienced as e.g. Clinical Trial Assistant or Clinical Trial Documentation Specialist
- Fluent in English
Skills:
- Clinical trial assistant
Keywords: Clincal Trial Assistant