Senior Statistical Programmer

Job Summary

Working remotely, the full-time Senior Statistical Programmer will prepare analysis programs for clinical data, coordinate statistical programming activities across multiple projects, and ensure compliance with regulatory standards while mentoring less experienced programmers.

Key responsibilities

• Develop algorithms and write programs to create datasets, producing data listings, summary tables, and graphs
• Prepare clinical trial datasets for regulatory submission and maintain a comprehensive understanding of CDISC standards
• Interact with project teams and manage the data warehouse for clinical study data

Required qualifications

• Bachelor's degree in statistics, computer science, or a related field with 5+ years of statistical programming experience
• 3+ years of experience in clinical statistical programming within the medical device, biotechnology, or pharmaceutical industries
• Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, and SAS/STAT; SAS Certified Base and/or Advanced Programmer preferred
• Knowledge of clinical data standards such as CDASH, SDTM, and ADaM
• Experience with regulatory submissions and clinical data management systems is a plus