
This senior statistical programmer role is a sponsor-dedicated position embedded within a global pharmaceutical client, offering a hybrid work arrangement requiring three days per week in Pennsylvania or New Jersey. The position leverages advanced SAS programming and CDISC standards to support early and late-stage clinical trials across various therapeutic areas. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex efficacy and safety analyses, creating submission documents, and leading programming standards development. The role appeals to candidates seeking autonomy and ownership while contributing to patient treatment innovation. It offers a collaborative culture that values scientific rigor, intellectual curiosity, and continuous professional development within a globally dispersed team environment.










