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Posted by: CCSI Inc - Robert Ryder <robert@ccsiinc.com> on October 28, 2009 at 13:49:58. Click here to reply to this post via Email.

Contract / Temp to Perm / Permanent: Contract
City: Santa Rosa
State: California
Country: United States

22942- Conducts analysis of systems specifications ,Gathers information from system users, Prepares system and programming documentation ,Develops code according to specifications and conducts unit testing

Plans and coordinates programming, testing, and documentation of statistical programs for use in creating statistical tables, graphics, and listing summaries. Programs analysis database manipulations and transfers of data for internal and external clients. May integrate databases from multiple studies or sources. Develops listing and table specifications with study Biostatistician. Interact with Data Management and Biostatistics staff and SP team members to negotiate timelines, responsibilities, and deliverables. Understands and complies with Standard Operating Procedures and Work Instructions. Programs, tests, and documents statistical programs and tools in accordance with SP standards and validation procedures. Meets milestones as assigned. Performs other duties as directed by Statistical Programming management. Will be working on Endovascular trials; position belongs to Vascular Biostat and data management group. Experience using SAS for more than 2 years and using SAS on clinical trial data analysis. Industrial experience is preferred Regulatory submission experience is a plus Prefer the candidate has industry experience and had experience with PMA submission etc. Absolute skill is SAS programming skills inlcuding SAS BASE/STAT/MACRO/SQL etc.

Must have experience in medical device, Pharma, research institutes, clinical or medical facilities.