
This senior statistical programmer role is a sponsor-dedicated position embedded within a global pharmaceutical client, supporting early and late-stage clinical trials. The position requires advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and complex efficacy and safety reports. Key responsibilities involve performing data manipulation, developing global programming standards, creating submission documents, and collaborating with cross-functional teams. The role offers a hybrid work arrangement in Pennsylvania or New Jersey, three days on-site. It is appealing for its focus on innovation, intellectual curiosity, and the opportunity to work autonomously on cutting-edge patient treatment research within a supportive culture that values scientific rigor and professional development.








