Director, Statistical Programming, Pharmacometrics

Role: Lead strategic pharmacometrics programming for clinical development programs across multiple therapeutic areas, supporting data analysis, regulatory submissions, and departmental standardization. Responsibilities: oversee programming strategies, implement tools and methodologies, coordinate activities with cross-functional teams, manage data integration for pharmacometric analyses, validate electronic submission deliverables, develop talent, and drive process improvements. Requirements: Master's degree in Statistics, Computer Science, Mathematics, Engineering, or related field; 12+ years supporting clinical trial data in biotech or pharma; expert SAS programming skills; experience leading teams of 4+; strong understanding of pharmacometrics, biostatistics, clinical reporting, and regulatory standards; experience with CDISC standards. Preferred: SAS Certification. HighValue: extensive SAS expertise in clinical development, leadership experience, and knowledge of regulatory submission processes. WorkSetup: On-site in Tarrytown, NY, four days/week.