As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills to support or lead one or more Phase I-IV clinical trials, with a focus on any of the following studies; Immunology, Oncology, Cardiovascular, Infectious Disease, Early Development, or Medical Affairs.

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
• Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s)
• Generating complex ad-hoc reports
• Preparing and validating submission packages
• Applying your strong understanding/experience with Efficacy analysis
• Preparing submission packages
• Performing lead duties when called upon
• Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
• Being adaptable and flexible when priorities change