Statistical Analyst (Hybrid)

Role: Statistical Analyst supporting pharmaceutical research and development, primarily focused on analyzing and reporting clinical trial data. Responsibilities include leading statistical programming for routine studies, developing and validating SAS programs for ADaM datasets, generating tables, listings, figures, and data visualizations, and preparing documentation for regulatory submissions. The analyst collaborates with Statistics, Clinical Data Strategy & Operations, and Development Operations teams. Qualifications: MS in Statistics, Computer Science, or related field with 2+ years of relevant experience, or BS with 4+ years; experience in pharmaceutical clinical trials; solid SAS programming skills, including ADaM dataset creation and validation; understanding of CDISC standards and drug development processes. Preferred: ability to support efficacy analyses across therapeutic areas and phases. HighValue: clinical trial data analysis in pharma R&D, SAS programming, ADaM datasets, regulatory documentation, GxP compliance. WorkSetup: not specified; role involves routine analytical activities with potential cross-functional interactions.