Description
We are looking for a
SAS Expert / CDISC (m/f)
Reference: -en
Start: 06/14
Duration: 6 MM++
Place: in Hessen
Branch: Pharmazeutische Industrie
Your tasks:
- Integration of clinical studies with CDISC Standards (SDTM and ADaM)
- Preparation of TFLs (Tables, Figures and Listings for clinical studies)
- Clinical Data Validation
Your qualifications
- Project experience within pharmaceutical industry
- Deep SAS-Knowledge
- Able to analyse and evaluate clinical study data
- Proficient in SAS Macro, SAS Graph, ProgReport, CDISC, SDTM and ADaM
Skills:
- Software developer
- Clinical data manager