Positions range from junior to senior levels. Responsible for editing and validating programs using SAS macros to generate listings and tables for the study reports and NDA submissions, data step manipulations for data quality assurance/validation of table, listing and summaries, using SAS to analyze clinical data from CRF's creating SAS data sets for the purpose of analysis and report writing for clinical trials (Pre-clinical through Phases IV), generating efficacy and safety reports, creating datasets and generating reports using PROC Tab, PROC Report, Data Null, SAS arrays, PROC SQL and Macros, and verify and document programs. Minimum Requirements: BS in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth). 3-5 years (10 years for Director, Statistical Programming) experience programming and analyzing scientific data, preferably in a pharmaceutical/clinical trial environment. Expertise in SAS programming language with a knowledge of relational databases, medical terminology and understanding of clinical research process. Level and title will be commensurate with the education and experience level of the selected candidate.