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: 63 days ago
Freshness: Confirmed live yesterday
Nearby: 99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $203k

This role $145k

$90k most similar roles pay here $295k

This role pays less than 91% of similar roles. Most pay $175,462–$231,000 — the shaded band above. At the midpoint, this role pays about $145k versus about $203k 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 57 open roles on FindRole.

Listed pay typically runs $134,400–$219,200 across 45 roles with salary data.

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At a glance

TL;DR · Principal Statistical Programmer

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The Principal Statistical Programmer joins the Statistical Programming team to provide leadership and support for processing clinical trial data across a diverse portfolio. This role involves designing and testing program logic, creating and maintaining programming specifications for analysis datasets, and ensuring high-quality documentation in a regulated environment. The individual will manage the quality control of analysis datasets, tables, listings, and graphs while coordinating timelines with a multidisciplinary study team to support reporting through regulatory approval. Key responsibilities include supporting submission requirements like annotated CRFs and define documents, as well as handling complex data for presentations and ad hoc requests. The position requires a Master's degree and experience in programming clinical study data, strong documentation skills, and the ability to contribute to tool development and process improvement within the department’s working groups.

Skills

Statistical Programming Clinical Trial Data Analysis Datasets Tables Listings Graphs Programming Specifications Annotated CRFs Quality Control Documentation

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.

Similar roles

Principal Statistical Programmer

Regeneron

Warren, NJ +1 63 days ago $109,900–$179,300

Statistical Programming Clinical Trial Data Analysis Datasets Tables Listings Graphs Programming Specifications Annotated CRFs Quality Control Regulated Environment Documentation

3+ yrs exp

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