& Provide SAS and other programming support with respect to design, conduct & Analysis of clinical trials. Create SAS analysis databases, summary tables and graphs for presentations, manuscripts and reports. Write and document SAS production macro code that can be used for a wide variety of applications. Develop SAS programs for statistical tables, data listings, and edit checks. Assist with Programming for editing and quality control of clinical trial data. And Documentation. Review CRFs, Data Management and Analysis Plans. Serve as the lead on a programming team. It will be the responsibility to ensure that work has been distributed appropriately and that all tasks are completed accurately and on time. Wynn Zheng 213 - 5078 (home) "shanghai88@rcn.com" shanghai88@rcn.com Work with Statisticians Programmers Medical doctor etc. Transforming data in various formats (ORACLE EXCEL CSV ASCII ACCESS ) into SAS datasets or reverse. Using SAS Microsoft Word EXCEL R etc. to do PK/PD Safety and Efficacy TLG for CSR NDA BLA. Using SAS and other software to do CDISC SDS & ADAM data set generating and maintaining data mining & data manipulating. Some QC & Documentation. Work with Statisticians Programmers Data Management Analysts Using SAS Microsoft Word HTML etc. to do Safety TLG for CSR NDA BLA. Using SAS and other software to do data transfer data mining & data manipulating. QC & Documentation. & Work with data analysts or other programmers in building or analyzing data files or providing survey support services. Prepare detailed specification from which programs will be written be able to translate requests into finished products without direct supervision take initiative and analyze, evaluate, test and code programs. May assist and supervise more junior programmers. Wynn Zheng 213 - 5078 "shanghai88@rcn.com" shanghai88@rcn.com
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