Manager, Statistical Programming, Pharmacometrics

Regeneron

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Tarrytown, NY
Salary
$128,600–$210,000 / yr
Employment
Full-time
Posted
3 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $189k
This role $169k
$117k most similar roles pay here $232k

This role pays less than 66% of similar roles. Most pay $160,217–$218,087 — the shaded band above. At the midpoint, this role pays about $169k versus about $189k for comparable roles.

Based on 240 similar postings.

Employer

About Regeneron

Regeneron is a leading science-driven biotechnology company that invents, develops, and commercializes life-transforming medicines for serious diseases.

Regeneron currently has 42 open roles on FindRole.

Listed pay typically runs $128,600–$219,200 across 32 roles with salary data.

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At a glance

TL;DR · Manager, Statistical Programming, Pharmacometrics

Manager, Statistical Programming, Pharmacometrics provides programming leadership supporting clinical development programs and pharmacometric analyses to inform critical development decisions. The role involves leading programming and quality control activities for analysis datasets, tables, figures, and listings across multiple projects while coordinating deliverables with cross-functional teams. Key responsibilities include creating and validating programming specifications, integrating data for exposure-response, population PK, and population PK/PD analyses, and supporting regulatory submissions, scientific publications, and conference presentations. The position requires advanced SAS programming expertise within a pharmaceutical environment and a strong understanding of pharmacokinetics, immunogenicity, and CDISC data standards. Candidates must possess 7-9+ years of experience in statistical programming to manage complex projects in a regulated environment. This role focuses on the technical execution of clinical pharmacology and drug development objectives through high-quality analysis and departmental process improvements.

What you'll do

  • 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 to support standardized analyses and reporting.
  • Integrate data across studies to support exposure-response, population PK, and population PK/PD analyses.
  • Support regulatory requests, scientific publications, and conference presentations through data-driven analyses.
  • Lead the creation and validation of electronic submission deliverables and supporting documentation.
  • Drive process improvements, standards development, and departmental initiatives to enhance efficiency and compliance.

What we're looking for

  • 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 pharmacokinetics, immunogenicity, exposure-response, and population PK methodologies.
  • Experience supporting clinical study reporting, regulatory deliverables, and CDISC data standards.
  • Experience in a pharma regulated environment (preferred).
  • 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.

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