Principal Programmer, Statistical Programming (Remote)

Role: Principal Statistical Programmer leading technical support and task delegation within clinical trial data analysis teams. Responsibilities include SAS programming, quality control of output, ensuring compliance with FDA/ICH regulations, and contributing to electronic submission documentation (eCTD, ISS/ISE). Engages with cross-functional teams including Biostatistics and Data Management, providing technical leadership and process improvements. Requirements: Bachelor's in a Scientific Discipline; 5+ years (M.S.) or 8+ years (B.S.) experience in biopharma or clinical research; proficiency in SAS, SAS Macro, SAS/STAT, SAS/GRAPH; knowledge of CDISC standards; regulatory submission experience. Preferred: deeper knowledge of clinical trials, GxP, and submission processes. HighValue: clinical development, regulatory compliance, SAS expertise, electronic submission (eCTD), cross-functional collaboration, remote/hybrid flexibility, salary range $149,200–$223,800, with potential bonuses and benefits.