Statistical Analyst (Hybrid)

Role: Statistical Analyst supporting pharmaceutical R&D, focusing on clinical trial data analysis and reporting. Responsibilities: lead routine statistical programming, develop SDTM/ADaM datasets per CDISC standards, create and validate analysis tables, listings, figures, and regulatory documentation, and contribute to macro development and data visualization. Requirements: MS in Statistics, Computer Science, or related field with 2+ years (MS) or BS with 4+ years of pharma experience; proficient in SAS programming and CDISC standards; experience with clinical trial datasets and regulatory submissions. Preferred: experience supporting efficacy analyses across phases and therapeutic areas; strong communication skills. HighValue: role is integral to drug development, supporting clinical trials with a focus on data standardization and regulatory compliance. WorkSetup: not specified; likely office-based or hybrid within a pharmaceutical R&D environment.