
This senior-level statistical programming 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, with a specific emphasis on early development, efficacy, and pharmacokinetic data. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data manipulation and analysis using SAS, creating submission documents, and ensuring adherence to CDISC standards. The role offers the appeal of working with autonomy on innovative patient treatments within a collaborative culture that values scientific rigor and intellectual curiosity. The work arrangement is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey.












