Manager, Statistical Programming, Pharmacometrics

Role: Manager, Pharmacometrics Programming, supporting clinical development with advanced statistical programming and analyses. Responsibilities: lead programming activities for datasets, tables, figures; ensure quality control; develop and validate programming specifications; integrate data for pharmacokinetics and pharmacometric analyses; support regulatory submissions, scientific publications, and presentations; lead creation of electronic submission documents; partner with cross-functional teams to deliver high-quality trial reports; drive process improvements and standards. Requirements: Bachelor's degree (Master's preferred); 7-9+ years in statistical programming within pharma or regulatory environment; advanced SAS expertise; strong understanding of pharmacometrics (PK, PD, exposure-response); experience supporting clinical reporting and regulatory standards (CDISC); excellent project management, communication, and collaboration skills. High-Value: clinical pharmacology, pharmacometric analyses, regulatory submissions, SAS programming, cross-functional collaboration, on-site in Tarrytown, NY, with a four-day workweek.