Develop and QC tables, figures, listings and derived datasets for RWE projects using SAS and SQL. Extract, manipulate, and manage large longitudinal healthcare datasets (claims, EMRs), optimize SAS macros, collaborate with Outcomes Research teams, mentor junior programmers, and follow project management procedures to deliver high-quality, reproducible results.

The Senior Programmer III will produce and validate datasets using SAS, mentor junior programmers, and ensure quality in clinical trial data management.

As a Statistical Programmer I, support statistical and programming teams in clinical trial reporting, generating datasets, and reviewing analysis plans while learning SAS programming.

As a Senior Programmer III, you will lead clinical programming efforts, support junior programmers, develop datasets using SAS, and ensure compliance with CDISC standards.

Senior statistical programmer responsible for designing and analyzing clinical studies, producing and QCing CDISC-compliant datasets and TLFs, providing peer review, ensuring regulatory compliance, managing project work and mentoring team members, and liaising with sponsors and lead statisticians.