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As a Senior Statistical Programmer, you will leverage SAS programming skills and CDISC standards to support clinical trials, perform data manipulation, and generate reports.

The Principal Statistical Programmer will generate datasets and reports, oversee CRO's programming deliverables, and ensure compliance with FDA regulations, while collaborating with various teams in clinical trials.

This role involves managing project operations, supporting leaders with scope reconciliations and invoicing, ensuring documentation compliance, and facilitating team collaboration.

The Principal Statistical Programmer develops and validates SAS and R programs, oversees CRO deliverables, and ensures high-quality statistical reporting for clinical trials.