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Responsibilities:

1. Analyze data and report statistical results.
2. Develop SAS programs to create SDTM datasets following CDISC SDTM standard with supervision.
3. 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.
4. Implement SAS programs to generate Define-XML package for FDA submission with supervision.
5. Develop SAS programmable edit checks to assist data monitoring, document and report data issue to Data Management with minimum supervision.
6. Perform other programming tasks as needed per management requests.

Qualifications: 1.Bachelor’s in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines required. 2.Proven knowledge and training in high-level computing languages such as SAS, C/C++, Java, R, Python, MATLAB and SQL. Database programming experience is a plus. 3.Detail oriented and ability to learn and adapt to changes. 4.Good verbal and written English. 5. Good team player and communicator. 6.Good working experience in Microsoft Office Suite, e.g., Word, Excel, PowerPoint, etc.