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As a Senior Statistical Programmer, you'll utilize advanced SAS skills and CDISC standards to support Phase I-IV clinical trials, performing data analysis and reporting while ensuring quality outputs and collaboration with teams.

The Senior Statistical Programmer will analyze clinical trial data, generate CDISC datasets, validate submissions, and collaborate with cross-functional teams.

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

The Principal Statistical Programmer oversees statistical programming for clinical trials, generates datasets and reports, and ensures high-quality deliverables while supporting regulatory submissions.