Pharmacometric Programming Lead (Regulatory Trials)

Regeneron Pharmaceuticals, Inc (USA); Village of Tarrytown (NY); On-site; USD 150,000 - 190,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Tarrytown, NY is seeking a Manager, Pharmacometrics Programming to provide programming leadership across clinical development and pharmacometric analyses.

You will lead analysis across projects, coordinate with study teams, and drive standardized reporting, data integration, and regulatory deliverables, contributing to high‑quality analyses and publications.

Qualifications

• Bachelor’s degree required; Master’s degree preferred.
• 7–9+ years of progressive experience in statistical programming.
• Advanced SAS programming experience within a clinical research or pharmaceutical environment.
• Strong understanding of pharmacometrics analyses, including PK, immunogenicity, exposure‑response, and population PK methodologies.
• Experience supporting clinical study reporting, regulatory deliverables, and CDISC data standards.

Responsibilities

• 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.

Education

Bachelor's degree

Master's degree

Tools

SAS

Job description

Regeneron Pharmaceuticals, Inc. in Tarrytown, NY is seeking a Manager, Pharmacometrics Programming to provide programming leadership across clinical development and pharmacometric analyses.

You will lead analysis across projects, coordinate with study teams, and drive standardized reporting, data integration, and regulatory deliverables, contributing to high‑quality analyses and publications.