
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, ADaM, and complex efficacy and safety reports. Key responsibilities involve performing data manipulation, developing submission documents, and leading quality control efforts for oncology and pharmacokinetic studies. The opportunity is appealing due to the autonomy and ownership granted to employees, a culture that values scientific rigor and innovation, and access to consistent training and development. The role operates on a hybrid basis, requiring three days per week in Pennsylvania or New Jersey.





