Principal Statistical Programmer

Role: Principal Statistical Programmer supporting clinical trial data processing and analysis within a biopharma setting. Objectives include leading programming activities, ensuring high-quality documentation, and supporting regulatory submissions across clinical studies. Responsibilities encompass programming analysis datasets, tables, listings, and graphs; creating specifications; validating submission components such as annotated CRFs; and contributing to process improvements within multidisciplinary teams. Requirements: Master's degree with 3+ years' relevant experience, proven programming support for clinical data, strong documentation and QC skills in regulated environments, and effective collaboration skills. Preferred: experience with regulatory submission support. High-Value: supporting clinical trial data analysis, quality control, and documentation in a regulated environment; working within a cross-functional team; supporting regulatory filings and submissions. Work setup: onsite in Warren, NJ or Cambridge, MA; no travel specified.