工作內容:
1. Familiar with SAS program (Macro, etc.) 2. Develop the statistical section of clinical trial protocol & report. 3. Develop SDTM and ADaM specification and datasets for FDA submission 4. Preparing analysis plans/report (SAP/SAR) (Statistical Analysis of clinical data, including PK) and writing detailed specifications and shell for analysis files, tables, listings and figures 5. Present and Interpret statistical results. 6. SOP development of related tasks. 7. Tasks assigned by the company