Statistical Analyst (Hybrid)

Role: Statistical Analyst supporting pharmaceutical research and development, focusing on clinical trial data analysis and reporting. Responsibilities: lead statistical programming for routine studies, develop documentation for regulatory submissions (reviewer guides, data definitions), create and validate ADaM datasets and statistical tables, listings, and figures using SAS, and develop data visualizations for communication. Requirements: MS in Statistics, Computer Science, or related field with 2+ years (MS) or BS with 4+ years relevant experience; hands-on SAS programming experience in drug development; familiarity with CDISC standards, ADaM datasets, and clinical trial processes. Preferred: experience supporting efficacy analyses across phases and therapeutic areas. HighValue: pharmaceutical clinical trials, regulatory documentation, SAS programming, ADaM data standards, GxP compliance. Collaboration: interfaces with Statistics, Clinical Data Strategy & Operations, and Development Operations. Work setup: not specified.