Manager, Statistical Programming, Pharmacometrics

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

Build our future together At Regeneron, we use data, science, and innovation to accelerate the development of transformative medicines. As a Manager, Pharmacometrics Programming, you will 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. You will also help advance departmental standards, improve processes, and strengthen programming capabilities that enable efficient and compliant drug development.

When & where Location: Tarrytown, NY Work Model: Four days per week on‑site

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.

This role requires 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.

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position. Salary Range (annually) $128,600.00 - $210,000.00

Regeneron is a leading biotechnology company that invents life‑transforming medicines for people with serious diseases. Founded and led for over 30 years by physician‑scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories.

Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.

Regeneron is also proud of award‑winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.