Associate Director, Biostatistics, Genetic Medicine

Regeneron

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Hybrid

Quick summary

Work type: Hybrid
Location: Tarrytown, NYWarren, NJ
Salary: $176,100–$287,300 / yr
Employment: Full-time
Posted: 55 days ago
Freshness: Confirmed live today
Nearby: 99+ roles within 25 mi

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $202k

This role $232k

$126k $305k

below market most similar roles pay here above market

This role pays more than 73% of similar roles. Most pay $167,625–$236,217 — the blue band above. At the midpoint, this role pays about $232k versus about $202k 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 73 open roles on FindRole.

Listed pay typically runs $134,400–$241,200 across 46 roles with salary data.

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At a glance

TL;DR · Associate Director, Biostatistics, Genetic Medicine

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The Associate Director, Biostatistics - Genetic Medicine joins the Biostatistics team to lead efforts across cross-functional groups. This role involves articulating drug development questions, assessing endpoint feasibility, and framing statistical approaches to design clinical experiments and interventional studies. The incumbent will lead the development of training for non-statistical colleagues, oversee less experienced statisticians, and represent statistical issues in regulatory agency meetings. Key responsibilities include drafting analysis plans, reviewing TFLs, and authoring SOPs. Required expertise includes a PhD or MS in statistics/biostatistics with specific years of pharmaceutical experience, knowledge of drug discovery, and proficiency in statistical software. The role specifically addresses the technical challenges of clinical trial development, requiring experience in Time to Event analysis and therapeutic areas such as Hematology, IO, or Multiple Myeloma.

Skills

Biostatistics Statistical Analysis Clinical Trial Design TFLs Time to Event (TTE) Statistical Software SOPs Drug Development Data Management Statistical Methodology

What you'll do

Design clinical experiments and interventional studies to generate and analyze data for drug development.
Frame statistical approaches and assess the feasibility of endpoints to address drug development questions.
Represent the Biostatistics department in regulatory agency meetings and prepare supporting materials.
Mentor and oversee less experienced statisticians and manage full-time staff.
Develop and deliver training on statistical concepts to non-statistical colleagues.
Author new or revised SOPs and lead process improvement and technical working groups.
Evaluate software appropriateness and research innovative statistical methodologies for clinical trial development.
Prepare and present written reports and findings to project teams, management, and regulatory agencies.

What we're looking for

PhD in statistics/biostatistics with over 6 years of pharmaceutical industry experience.
MS degree in statistics/biostatistics with over 11 years of pharmaceutical industry experience.
Solid knowledge of statistical analysis methodologies, experimental design, and clinical trial design.
Expertise in statistical software.
Excellent influence, leadership, and cross-functional collaboration skills.
Demonstrated critical thinking, time management, and effective communication skills.
Experience in Hematology, IO, non-oncology, Multiple Myeloma, or similar therapeutic areas (preferred).
Time to Event (TTE) experience (preferred).

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