Beschreibung
We are looking for a
Trial Documentation Specialist (m/f)
Reference: -en
Start: ASAP
Duration: 12 MM++
Place: in the Basel region
Branch: Herstellung von pharmazeutischen Erzeugnissen
Your tasks:
- Close collaboration with multiple CRAs, working on studies covering Europe and Asia Pacific
- Manage and review the TMF and eTMF based documentation with regard to completeness and quality
- File and archive documentation in accordance with respective regulations
Your qualifications
- University degree, ideally with a Life Sciences focus
- Profound experience in working with and handling clinical trial documentation
- Profound knowledge regarding TMF and eTMF
- Outstanding English skills in both verbal and written form
Skills:
- CRA
Keywords: CRA