• Analyze data and report statistical results. • Develop SAS programs to create SDTM datasets following CDISC SDTM standard with supervision. • Develop, debug, maintain SAS programs and macros to create Tables, Listings and Graphs for Clinical Study Report following CDISC, industry guidelines and Statistical Analysis Plan with supervision. • Implement SAS programs to generate Define-XML package for FDA submission with supervision. • Develop SAS programmable edit checks to assist data monitoring, document and report data issue to Data Management with minimum supervision. • Perform other programming tasks as needed per management requests.