Manager, Statistical Programming, Pharmacometrics

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.

• 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.

• 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.

Does this sound like you? 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…