
This senior-level role places a statistical programmer fully embedded within a global pharmaceutical client's team to support early and late-stage clinical trials. The position requires advanced SAS programming expertise to generate and validate CDISC-compliant deliverables, including SDTM and ADaM datasets, as well as efficacy and safety analysis reports. Key responsibilities involve designing complex programming algorithms, performing data manipulation for pharmacokinetic studies, and leading quality control processes for submission documents. The opportunity is appealing due to the autonomy and ownership granted to individuals driving patient treatment innovation within a collaborative culture that values scientific rigor and intellectual curiosity. The role operates on a hybrid basis, requiring three days per week on-site in Pennsylvania or New Jersey, with strong support from the parent organization for professional development.
















