Statistical Analyst - ADaM Programming (Hybrid)

Role: Statistical Analyst supporting pharmaceutical R&D, specializing in clinical trial data analysis and reporting. Responsibilities: lead statistical programming for routine studies, develop documentation for regulatory submissions, create and validate ADaM datasets, produce Tables, Listings, and Figures, and develop data visualizations. Collaborate with Statistics, Data Strategy & Operations, and Development teams. Requirements: MS in Statistics, Computer Science, or related field with 2+ years (MS) or BS with 4+ years of relevant experience; practical SAS programming experience in drug development; familiarity with ADaM datasets and CDISC standards; strong communication skills. Preferred: experience supporting efficacy analyses across phases and therapeutic areas. High-Value: clinical trials, pharmaceutical development, ADaM data standards, SAS programming, regulatory documentation, cross-functional collaboration. WorkSetup: not specified, but implied to be based in a corporate or research environment.