Performs all SAS programming required for clinical trial analysis and reporting; Ensures that activities and processes performed are conducted according to sponsor requirements; Works closely with the Biostatistics and Data Management departments on various clinical projects; Leads programming efforts for large complex studies; Requires time management skills, and strong SAS programming expertise; Reviews case report form (CRF) design; Designs and/or reviews database structure; Writes edit checks from the Data Cleaning Plan (DCP) specifications; Creates derived-analysis datasets; Executes analyses specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plans (RAP) under the guidance of the project statistician; Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR); Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses. It is preferred that the candidate is familiar with Unix platform and/or CDISC standards. Candidate MUST be able to complete a 1 year assignment. No OT, No Travel required. All work to be performed onsite in Madison.