
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 across various therapeutic areas, including oncology. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data manipulation and efficacy analysis using SAS, and preparing submission documents like eCRTs and Define.XML. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and intellectual curiosity. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, providing a balance of remote flexibility and collaborative team interaction.










