1. Be responsible for study level DM SAS programming and testing in clinical trials.

2. Review or develop DM documents include but not limited eCRF, Edit Check Specification, Data Transfer Agreement, SDTM documents and so on following SOPs

3. Develop SAS program for non-EDC edit checks, listings for data review, external data integration and reconciliation etc.

4. Create SDTM aCRF, Mapping Specification, metadata, SDRG etc. for SDTM package. Develop SAS program for SDTM package and QC of SDTM package

5. SAS macro development

Requirements:

1. Years of SAS programming experience or fresh graduate showing high potential.

2. Education: Bachelor or Master Degree in Biostatistics, Statistics, Epidemiology, Mathematics, or Computer Science other scientific field (or equivalent theoretical/technical depth).

3. Logical thinking.

4. Good at communication, learning, with a proactive attitude.

5. Familiar with MS office.

6. Good in Oral and writing English

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