Senior Pharmacometrics Programming Lead

Regeneron Pharmaceuticals; Tarrytown (GA); On-site; USD 129,000 - 210,000; Full time

Job summary

Regeneron Pharmaceuticals in Tarrytown, NY is seeking a Manager, Pharmacometrics Programming to provide programming leadership supporting clinical development programs and pharmacometric analyses that inform critical development decisions.

This role offers the opportunity to work across multidisciplinary teams, contribute to regulatory submissions, and drive the delivery of high-quality analyses that support clinical pharmacology and development objectives.

Qualifications

• Bachelor’s degree required; Master’s preferred.
• 7–9+ years of progressive experience in statistical programming.
• Advanced SAS programming in pharma.
• Experience supporting regulatory deliverables and CDISC.
• Strong PM, communication, problem-solving, and cross-functional collaboration skills.

Responsibilities

• Lead programming and QC 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 for standardized analyses and reporting.
• Integrate data across studies to support exposure‑response and population PK analyses.
• Support regulatory requests, data‑driven analyses, publications, and conference presentations.
• Lead creation/validation of electronic submission deliverables and documentation.
• Partner with multidisciplinary study teams to deliver high-quality clinical trial analyses and reports.
• Drive process improvements, standards development, and departmental initiatives to enhance efficiency and compliance.

Skills

Advanced SAS

Pharmacometrics

Statistical programming

Cross-functional collaboration

CDISC data standards

Education

Bachelor’s degree

Master’s degree

Tools

SAS

Job description

Regeneron Pharmaceuticals in Tarrytown, NY is seeking a Manager, Pharmacometrics Programming to provide programming leadership supporting clinical development programs and pharmacometric analyses that inform critical development decisions.

This role offers the opportunity to work across multidisciplinary teams, contribute to regulatory submissions, and drive the delivery of high-quality analyses that support clinical pharmacology and development objectives.