Statistical Analyst (Hybrid)

Role: Statistical Analyst supporting clinical trial data analysis in pharmaceutical R&D, focusing on routine study programming and regulatory documentation. Responsibilities: lead statistical programming activities, develop and validate ADaM data sets and analysis outputs following CDISC standards, create data visualizations, and prepare documentation for regulatory filings such as reviewer guides and data definitions. Interface with Statistics, Data Strategy & Operations, and Development Operations. Qualifications: MS in Statistics, Computer Science, or related field with 2+ years (MS) or BS with 4+ years of relevant experience; experience with SAS programming, ADaM data creation, and pharmaceutical clinical trials. Preferred: ability to support efficacy analyses across phases and therapeutic areas; strong communication skills. HighValue: experience with drug development, regulatory documentation, CDISC standards, and GxP compliance. WorkSetup: not specified; role involves collaboration across multiple research functions.