The Statistician is responsible for providing statistical analyses and summaries of studies in support of product development and PMA, BLA and NDA submissions. He/she will review the statistical analysis sections of clinical protocols, write statistical analysis plans, prepare table and listing shells, create randomization schedules, review CRFs and Data Management Plans, and conduct statistical analyses. The Statistician will work with SAS programmers and provide specifications of necessary analyses and summaries. He/she will be responsible for developing SAS programs and overseeing quality control activities to ensure the accuracy of the final results summaries produced by the SAS programmers.