Manager, Statistical Programming, Pharmacometrics

BioSpace; Village of Tarrytown (NY); On-site; USD 129,000 - 210,000; Full time

Job summary

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

You will work across multidisciplinary teams, contribute to regulatory submissions, and drive high-quality analyses while advancing standards and efficiency.

This role requires a Bachelor's degree, 7–9+ years in statistical programming in pharma, advanced SAS, and strong cross-functional collaboration.

Qualifications

• Bachelor's degree required; master's preferred.
• 7–9+ years of progressive statistical programming experience in pharma.
• Advanced SAS programming in a regulated environment.
• Strong pharmacometrics knowledge: PK, PK/PD, exposure–response.
• Experience with regulatory deliverables and CDISC data standards.
• Excellent project management and cross-functional collaboration.

Responsibilities

• Lead programming and QC for analyses across projects.
• Coordinate pharmacometrics activities with cross-functional teams.
• Create, maintain, and validate programming specifications for standardized analyses.
• Integrate data across studies for PK/PKPD analyses.
• Support regulatory requests, data analyses, publications, and conferences.
• Lead creation and validation of electronic submission deliverables.
• Partner with study teams to deliver high-quality analyses and reports.
• Drive process improvements and standards development.

Skills

SAS programming

Pharmacometrics

Regulatory environment

Project management

Cross-functional collaboration

Education

Bachelor's degree

Master's degree preferred

Tools

CDISC standards

Electronic submission tools

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

Discover your role

• 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.

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 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. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

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