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Job DescriptionRole PurposeProvide hands‑on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company standards. The Principal Statistical Programmer is expected to work independently, deliver high‑quality programming deliverables, and collaborate effectively with Biostatistics and Clinical Data Management.Key ResponsibilitiesPrimary ResponsibilitiesDevelop complex analysis datasets, specifications, and summary outputs tables, listings, figures, and graphs for inclusion in clinical study reports, regulatory submissions, and internal presentations.Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure efficient programming, reporting, review, and traceability.Perform independent program review and validation, ensuring complete, accurate, and inspection‑ready documentation in compliance with applicable regulations and internal procedures.Support ad hoc and planned analyses in collaboration with the designated statistician, including responses to data review questions.Partner with Clinical Data Management and Biostatistics to review CRFs, database specifications, edit checks, and data derivations as needed.Proactively identify programming risks, data issues, or efficiency opportunities and communicate them clearly to study team members.Scope & Level of IndependenceWorks independently with minimal supervision, receiv