
This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data manipulation for efficacy and safety analyses, and creating submission documents. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.










