Biostatistician with Expert Knowledg in Cdisc and Blind Data Review (m/f)

- Oversight and responsibility of ou outsourced activites (preparation of electronic submissions)
- Participate in blind data review meetings
- Programming the analysis of pre-clinical and clinical trials
- Development of study designs and study protocols
- Develop and review statistical analysis plans
- Program in-house analysis (derived datasets, tables and listings) with SAS
- Develop datasets for electronic submissions (SDTM, ADaM )
- Creation of submission documents and process authorities' requests
- Diploma in Statistics or Mathematics or related field
- Profound experience as a biostatistician for clinical trials in the pharmaceutical industry
- At least intermediate experience of SAS programming (including macro language) and experience in using NQuery Advisor for sample size calculations
- Expert in CDISC standards
- Good understanding of global clinical trial practices
- Good team player, good business ethics
- Very good English (oral and written), German would be an advantage

Weitere Qualifikationen: Biostatistician