
This senior-level role places a statistical programmer fully embedded within a global pharmaceutical client's team, supported by Cytel's internal 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 efficacy and safety data analysis, and creating submission-ready documents. The role appeals to candidates seeking autonomy and ownership in a culture that values scientific rigor, innovation, and intellectual curiosity. The work arrangement is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.















