Associate Director Statistical Programming - Pharmacometrics

Role: Associate Director of Pharmacometrics Programming, leading programming efforts for clinical pharmacology data analysis supporting drug development and regulatory submissions. Responsibilities: oversee programming and QC of analysis datasets, facilitate data integration across studies (e.g., Exposure-response, PopPK), support electronic submission requirements, and collaborate with multidisciplinary teams for clinical report generation. Manage project timelines, resources, and standards compliance. Requirements: Master’s in Statistics, Computer Science, Mathematics, Engineering, or Life Sciences; 10+ years of SAS programming experience in biotech/pharma, with expertise in clinical trial data processing, biostatistics, and PK/PD analyses. Skills in SAS (Base, Macro, Graph), R, Python, relational databases, CDISC standards, and data sciences (including AI use cases). Preferred: experience in project and people management, therapeutic area expertise, SAS Certification. HighValue: 10+ years in clinical data programming, extensive SAS skills, experience with regulatory data standards, and support of clinical pharmacology analyses. Work setup: 4 days onsite in Tarrytown, NY or Warren, NJ.