Principal Statistical Programmer, Genetic Medicines

Regeneron

Confirmed live today High trust

Quick summary

Work type: On-site
Location: Warren, NJCambridge, MA
Salary: $109,900–$179,300 / yr
Employment: Full-time
Posted: 2 days ago
Freshness: Confirmed live today
Nearby: 31 roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $209k

This role $145k

$92k $278k

below market most similar roles pay here above market

This role pays less than 91% of similar roles. Most pay $170,875–$246,700 — the blue 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 69 open roles on FindRole.

Listed pay typically runs $134,400–$241,200 across 55 roles with salary data.

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At a glance

TL;DR · Principal Statistical Programmer, Genetic Medicines

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The Principal Statistical Programmer - Genetic Medicines joins the Statistical Programming team to support a study team across the clinical portfolio. This role involves providing programming leadership and support for processing clinical trial data, including the creation and validation of analysis datasets, tables, listings, and graphs. Key responsibilities include designing and testing program logic, maintaining high-quality documentation in a regulated environment, and creating programming specifications for analysis datasets. The candidate must demonstrate strong documentation and quality control skills while collaborating within a multidisciplinary study team to support analysis and reporting through regulatory approval. The work focuses on clinical study data and analysis deliverables, requiring the ability to handle complex data, participate in tool development, and manage shifting timelines for genetic medicines.

Skills

Statistical Programming Clinical Trial Data Analysis Datasets Tables Listings Graphs Programming Specifications Annotated CRFs Quality Control Tool Development Process Improvement

What you'll do

Lead programming and quality control for analysis datasets, tables, listings, and graphs.
Create and maintain programming specifications for analysis datasets across various 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.
Participate in department working groups to contribute to tool development and process improvement.
Communicate shifting timelines and milestones clearly to the multidisciplinary study team.

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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