Responsibilities:
1. Analyze data report statistical results.
2. Develop SAS programs to SDTM datasets following CDISC SDTM standard with supervision.
3. Develop, debug, maintain SAS programs macros to Tables, Listings Graphs fClinical Study Report following CDISC, industry guidelines Statistical Analysis Plan with supervision.
4. Implement SAS programs to generate Define-XML package fFDA submission with supervision.
5. Develop SAS programmable edit checks to assist data monitoring, document 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 related scientific
disciplines required.
2.Proven knowledge training in high-level computing languages such as SAS, C/C++, Java, R, Python, MATLAB SQL. Database programming experience is a plus.
3.Detailiented ability to learn adapt to changes.
4.Good verbal written English.
5. Good team player communicator.
6.Good working experience in Microsoft Office Suite, e.g., Word, Excel, PowerPoint, etc.
更新于 2025-09-03