- Write statistical programs for use in creating analysis datasets, tables, listings, and figures;
- Review analysis plans for appropriate methods;
- Program study analyses and review study results;
- Communicate the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis
- Master’s Degree
- Industry working experience with SAS programming, or SAS certificate
- Knowledge of databases and data management process;
- Knowledge of statistical methods commonly used in pharmaceutical clinical trials.