Job Description
Job Description
Qualifications
Please submit your CV in English.
You will contribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets and summaries.
You will:
- Develop analysis data sets structure
- Develop program requirements and specifications
- Be involved in SAS programming of ADS and Tables, Listings and Figures
- Support SAS program validations
- Prepare and review program documentation
- Produce TFL
- Communicate with project teams and company departments with regard to statistical programming of clinical research projects
Qualifications
- University and Master's degree in Statistics or Biostatistics
- Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) an...