Principal Statistical Programmer

Regeneron

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Warren, NJCambridge, MA
Salary
$109,900–$179,300 / yr
Employment
Full-time
Posted
61 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $209k
This role $145k
$90k most similar roles pay here $295k

This role pays less than 93% of similar roles. Most pay $180,500–$237,387 — the shaded band above. At the midpoint, this role pays about $145k versus about $209k 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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View all roles at Regeneron

At a glance

TL;DR · Principal Statistical Programmer

The Principal Statistical Programmer joins the Statistical Programming team to provide leadership and support for processing clinical trial data across a diverse portfolio. This individual will be responsible for designing and testing program logic, creating and maintaining programming specifications for analysis datasets, and ensuring high-quality documentation in a regulated environment. Day-to-day tasks include managing quality control for tables, listings, and graphs, coordinating with multidisciplinary teams to meet shifting timelines, and supporting submission requirements like annotated CRFs and define documents. The role also involves contributing to tool development and process improvement within department working groups. Candidates must possess a master's degree and experience in programming clinical study data and analysis deliverables. This position focuses on the technical challenges of preparing clinical trial data for regulatory approval and subsequent product launch.

What you'll do

  • Lead the programming and quality control of analysis datasets, tables, listings, and graphs.
  • Create and maintain programming specifications for analysis datasets across multiple studies.
  • Support the creation and validation of submission requirements, including annotated CRFs and define documents.
  • Design and test program logic independently while maintaining documentation in a regulated environment.
  • Provide programming support for presentations and complex statistical ad hoc requests.
  • Coordinate activities and communicate shifting timelines and milestones to the study team.
  • Contribute to department working groups focused on tool development and process improvement.

What we're looking for

  • 3+ years of relevant experience.
  • Proven programming experience supporting clinical study data and analysis deliverables.
  • Strong documentation and quality control skills within a regulated environment.
  • Experience collaborating within a multidisciplinary study team.
  • Master's degree.

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