
This senior statistical programmer role involves working fully embedded within a global pharmaceutical client to support early and late-stage clinical trials. The position requires leveraging advanced SAS programming skills and CDISC standards to generate, validate, and analyze statistical deliverables including SDTM, ADaM, and efficacy reports. Key responsibilities include performing data manipulation for safety and efficacy, creating complex ad-hoc reports, and leading submission document preparation. The role is appealing due to the opportunity to work with autonomy on innovative patient treatments within a collaborative culture that values scientific rigor and intellectual curiosity. The position is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey, with access to consistent training and development support.





