About the job
Please submit your CV in English.
As a SAS Programmer I, you will play a crucial role in statistical programming for global clinical trials. Collaborating closely with international teams of statisticians, programmers, and data managers, you will be responsible for programming data sets and creating summaries.
Your responsibilities will include:
- Designing the structure of analysis data sets
- Creating program requirements and specifications
- Engaging in SAS programming of Analysis Data Sets (ADS) and generating Tables, Listings, and Figures (TFL)
- Assisting with SAS program validations
- Preparing and reviewing program documentation
- Communicating effectively with project teams and various departments regarding the statistical programming of clinical research projects

