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Monday, January 12, 2009

Immediate Clinical SAS Role in NJ

Central NJ Position Type: Contract Details: Our client is a midsize pharmaceutical organization that requires a senior level contract SAS programmer work within their Inflammation Group. The Senior SAS programmer will provide statistical programming technical leadership and support to Data Management. This individual will participate in the design, development, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical data for phase ll studies. - Codes complex SAS programs for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDlSC SDTM format. The SAS programmer should have advanced experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH. Experience with EDC system is required, preferably Inform. Requirements: BS in Statistics or Computer Sciences 5-8 years Clinical SAS programming EDC / Inform Please contact Beth Crowley at Orbis Data Solutions for more details: Contact (email): bcrowley [at] orbsidata.com