
This senior statistical programmer role is embedded within a global pharmaceutical client, focusing on early and late-stage clinical trials in the pharmaceutical and biotech sectors. 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 data manipulation, PK/PD modeling, creating submission documents, and leading quality control processes. The role offers a hybrid work arrangement in Pennsylvania or New Jersey, combining three days of on-site collaboration with remote flexibility. It appeals to candidates seeking autonomy and ownership within a culture that values scientific rigor, innovation, and intellectual curiosity, supported by consistent professional development and a collaborative global team environment.





