*6 years of SAS programming experience with 3.5 in clinical trials. *Lead programmer for Phase I - Phase IV clinical trials including integrated summaries of safety and efficacy *Responsible for the execution and summary of all required analyses specified in the statistical analysis plan as well as the creation of all derived SAS datasets *Programmed custom SAS and Visual Basic macros used departmentally wide to automate the creation of tables and listings, vastly improving the accuracy and efficiency of compiling clinical study reports *Created SAS training documents for new programmers and statisticians *Prepare and review necessary company and FDA documents including program requirements,verification plans and reports, and data specifications