
This senior statistical programmer role is a sponsor-dedicated position embedded within a global pharmaceutical client, requiring a hybrid work arrangement in Pennsylvania or New Jersey three days per week. The position involves leveraging advanced SAS programming and CDISC standards to support early and late-stage clinical trials, including generating and validating SDTM, ADaM, and TFL deliverables. Key responsibilities encompass data manipulation for safety and efficacy analysis, creating complex ad-hoc reports, and leading submission document preparation. The role appeals to candidates seeking autonomy and ownership within a collaborative culture that values scientific rigor and innovation. It offers opportunities for professional growth through consistent training and the chance to work on cutting-edge patient treatment programs.
















