I. Data Management - Design case report forms (CRFs) - Develop CRF completion guidelines (CCG) - Develop data validation plan (DVP) - Build data cleaning specification 1. Develop Edit Check 2. Logic Check Specifications 3. Validated clinical data by SAS program - Build up electronic data capture (EDC) - Develop datasets by SDTM rules - Conduct reconciliation of SAEs - Clean general queries - Maintain clinical study related documents - Coordinate with cross-function departments for study issues - Reviewed cross-function documents (e.g. protocol etc.) II. Statistical Programmer - Implement data manipulation into SAS programs and macros independently - Develop statistical analysis plan - Create data listings, statistical tables, and figures for clinical trial data - Maintain documents of SAS programs and validation results - Coordinate with cross-function departments for study issues

Health Data Analysis National Health Insurance Research Database SAS Programming