Principal Biostatistician, Hematology

Regeneron

Confirmed live yesterday High trust

Hybrid

Quick summary

Work type: Hybrid
Location: Sleepy Hollow, NYWarren, NJ
Salary: $109,900–$179,300 / yr
Employment: Full-time
Posted: 3 days ago
Freshness: Confirmed live yesterday
Nearby: 27 roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $180k

This role $145k

$96k $236k

below market most similar roles pay here above market

This role pays less than 75% of similar roles. Most pay $144,900–$214,500 — the blue band above. At the midpoint, this role pays about $145k versus about $180k 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 64 open roles on FindRole.

Listed pay typically runs $142,450–$241,200 across 50 roles with salary data.

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At a glance

TL;DR · Principal Biostatistician, Hematology

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The Principal Biostatistician - Hematology joins the Global Development team to lead statistical strategies for drug development. This role involves articulating development questions, assessing endpoint feasibility, and framing statistical approaches for clinical experiments and interventional studies. The incumbent will co-author clinical study protocols and statistical analysis plans, perform analyses for interim and final reports, and develop training for non-statistical colleagues. Key responsibilities include collaborating with Statistical Programming on tables, figures, and listings, as well as evaluating software for novel statistical methodologies. The position requires expertise in R or SAS, a PhD or MS in statistics/biostatistics, and deep knowledge of experimental and clinical trial design. The work focuses on analyzing data from clinical trials and non-trial sources to facilitate program-level decision-making within the hematology therapeutic area.

Skills

Biostatistics R SAS Clinical Trial Design Statistical Analysis Plans Statistical Methodology Data Analysis Clinical Study Protocols Statistical Programming Regulatory Reporting

What you'll do

Articulate drug development questions and assess the feasibility of clinical endpoints.
Design clinical experiments and interventional studies to generate and analyze data.
Co-author clinical study protocols and statistical analysis plans.
Perform statistical analyses for interim and final reports.
Develop and deliver statistical training to non-statistical colleagues.
Analyze data from clinical trials and non-trial sources to facilitate program-level decisions.
Prepare presentations and written reports to communicate results to management and regulatory agencies.
Research innovative statistical methods and applications for clinical trial development.

What we're looking for

PhD in statistics/biostatistics or related disciplines with internship experience.
MS degree in statistics/biostatistics with more than 5 years of experience as a statistician in the pharmaceutical industry.
Solid knowledge of statistical analysis methodologies, experimental design, and clinical trial design.
Expertise in statistical software such as R or SAS.
Excellent influence and leadership skills with a demonstrated ability to collaborate in a cross-functional environment.
Demonstrated critical thinking, time management, and effective communication skills.
Ability to work productively in a fast-paced collaborative environment.

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