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# Manager, Statistical Programming, Pharmacometrics

- **Company:** Regeneron
- **Location:** Tarrytown, NY, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Data Governance, SAS (Software)
- **Published:** October 2, 2026
- **Apply:** https://dejobs.org/x/x/558556B2294548BD835B0951411AAEB7/job/

## About the Role

* Bachelor's degree required; Master's degree preferred
 * Must have 7-9+ years of progressive experience in statistical programming. Experience in pharma regulated environment preferred.
 * Advanced SAS programming experience within a clinical research or pharmaceutical environment.
 * Strong understanding of pharmacometrics analyses, including pharmacokinetics, immunogenicity, exposure-response, and population PK methodologies.
 * Experience supporting clinical study reporting, regulatory deliverables, and CDISC data standards.
 * Strong project management, communication, problem-solving, and cross-functional collaboration skills.
 * Ability to manage multiple priorities while delivering high-quality work in a regulated environment.

## Description

* Lead programming and quality control activities for analysis datasets, tables, figures, and listings across multiple projects.
 * Coordinate pharmacometrics programming activities and deliverables with cross-functional teams and study stakeholders.
 * Create, maintain, and validate programming specifications that support standardized analyses and reporting.
 * Integrate data across studies to support exposure-response, population PK, and population PK/PD analyses.
 * Support regulatory requests, data-driven analyses, scientific publications, and conference presentations.
 * Lead creation and validation of electronic submission deliverables and supporting documentation.
 * Partner with multidisciplinary study teams to deliver high-quality clinical trial analyses and reports.
 * Drive process improvements, standards development, and departmental initiatives that enhance efficiency and compliance.