SAS Programmer

Tasks: Shall provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical statistical reports, etc. Contribute to the integrated clinical/statistical report and other similar docs. Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting. Perform QA procedures on work performed by others. Develop, test, validate, document, maintain and execute software and/or systems using the currently endorsed tools or support of production activities.
REQUIREMENTS
Experience: 3 years SAS. Minimum of BS degree. Pharma exp. is required with clinical trials knowledge. Comments: Data aggregation experience would be preferred, including assembling and reviewing existing documentation aggregating data from several studies into a common data set structure across domains, and providing supporting documentation.