o Support generation of dataset specifications. o Development of mapping specifications for integrated datasets.o Development and documentation of programs used to generate datasets.o Development and documentation of programs used to generate listings, tables and graphs.o Program validation including generation of validation documentation.o Data preparation and documentation according to CDISC data standards.o Intense and cross functional interaction with other members of the project team.o Perform all programming work in accordance with the SOPs.

 Protocol writing assists for statistical section such as statistical method, sample size calculation. Study database setup included: data validation rules built. Study database maintain included: data cleaning (issue detect and query) and data transfer. Wrote statistical analysis plan/TFL shell/CSR report and related programs. Tool development through programming. Prepare randomisation specifications and schedules, and liaise with EDC/eCRF vendors, or third parties, to set up IWRS randomisation where applicable. SAS programming of derived datasets, tables, listings and figures according to the SAP and mock templates. Assist Business Development in forecasting Statistic resource needs for new study bids. Prepare the file for TFDA and EMA GCP inspection Protocol writing assists for statistical section such as statistical method, sample size calculation.

 According to the incidence and mortality rate of kidney disease published that year, arrange free health kidney disease screening, school children lectures, community health education, medical guidance in Taiwan. In cooperation with hospitals and local public health center, free health screening and health education are provided to local residents. Provide the simple review submission to IRB, and regularly submit the interim reports. Ensure quality of statistical data and the participant's health report.

 Design the courses for dementia and mild cognitive impairment elders slowed disability. Application, examination and write-off of funds related to the plan of dementia. Assist in the planning of dementia care in long-term care 2.0 policies

 Served as education and training instructor to lecture about company's technology and product applications. Assisted clinical trials application and communication with CRO and CDE. Developed and implemented operation policies and procedures of procurement cycle. Supervised recruitment, hiring, training, and employee orientation.