RESPONSIBILITIES: 1.Deliver individual programming deliverables of projects with low to medium complexity. 2.Develop quality control checks for programs or output. 3.Develop programs to produce tables, listings, figures and other reports and analyses summarizing clinical trial results.4.Develop programs to produce electronic submission deliverables.5.Maintain documentation as appropriate.6.Participate in the development and review of study-specific procedures.7.Participate in clinical project team meetings as required.8.Assist in testing and implementation of new and updated internally and externally developed software as well as new SAS releases.9.Develop proficiency in technical/programming skills.EDUCATION AND EXPERIENCE REQUIREMENTS: 1.Master’s degree in computer science, mathematics or other scientific field +0 year experience or Bachelor’s degree in computer science, mathematics or other scientific field + 3 years ' experience programming and analyzing scientific data in pharmaceutical or biotechnology industry.2.Solid knowledge of SAS programming and/or other statistical software (e.g., S-Plus, R, PASS). 3.Good communication skills in written and oral English.