Principal Statistical Programmer

Role: Principal Statistical Programmer supporting clinical trial data processing and analysis across Regeneron's portfolio, contributing to regulatory submissions and study support. Responsibilities: lead or support programming and quality control of analysis datasets, tables, listings, and figures; develop and maintain programming specifications; support submission creation, validation, and documentation; collaborate within multidisciplinary teams to ensure timely delivery and quality through regulatory approval and launch; assist with presentations and ad hoc data requests; participate in process improvement initiatives and tool development. Requirements: Master's degree with 3+ years of relevant clinical data programming experience; strong documentation and quality control skills in a regulated environment; proven ability to support clinical study deliverables and collaborate across teams. HighValue: clinical trial data support, analysis dataset programming, submission documentation, collaboration in multidisciplinary teams, regulated environment expertise. WorkSetup: onsite in Warren, NJ or Cambridge, MA.