Principal Statistical Programmer Consultant

As a Principal Statistical Programmer Consultant, you will be working directly for a single sponsor while having the security and additional career opportunities. Main responsibilities include participating in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings; producing data listings, summary tables, and graphics for interim and final analyses; integrating data across studies within a project. You will also test, document, review, and validate all programs according to department guidelines, coordinate data transfer and/or programming standards with CROs and vendors, validate analysis datasets and TFLs from vendors, and collaborate with Biometrics functions for all activities related to the analysis of clinical trial data. The role involves the execution of ad-hoc requests, manuscripts, posters, and presentations.