
This senior statistical programmer role involves working fully embedded within a global pharmaceutical client's team to support early and late-stage clinical trials. The position requires leveraging advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM and ADaM datasets, as well as performing complex efficacy and safety analyses. Key responsibilities include developing global programming standards, creating submission documents, and collaborating with cross-functional teams to ensure data integrity. The opportunity is appealing due to the autonomy and ownership granted to employees, the chance to drive innovation in patient treatment, and a culture that values scientific rigor and intellectual curiosity. The role is hybrid, requiring three days of on-site work in Pennsylvania or New Jersey, with strong support and development resources provided by the parent organization.













