Senior Manager, Statistical Programming, Hematology

Regeneron

Confirmed live today High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Warren, NJCambridge, MA
Salary
$150,500–$245,500 / yr
Employment
Full-time
Posted
2 days ago
Freshness
Confirmed live today

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $185k
This role $198k
$126k $258k
below market most similar roles pay here above market

This role pays more than 68% of similar roles. Most pay $155,000–$214,900 — the blue band above. At the midpoint, this role pays about $198k versus about $185k 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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View all roles at Regeneron

At a glance

TL;DR · Senior Manager, Statistical Programming, Hematology

The Senior Manager, Statistical Programming - Hematology joins the Statistical Programming function to provide technical leadership across project teams within specific therapeutic areas. This role involves driving high-quality programming deliverables from single studies through regulatory approval and product launch while coordinating documentation and specifications. The successful candidate will lead programming support across multiple studies, communicate requirements to project teams, and serve as a subject matter expert on key topics. Responsibilities include mentoring junior programmers, guiding department goals, and managing concurrent priorities. Required skills include advanced SAS programming expertise in a clinical data environment, a strong understanding of clinical trial principles, and regulatory submission requirements. Candidates should possess a degree in a quantitative or life science discipline and experience in biotechnology or pharmaceutical clinical development. Knowledge of R or Python is preferred.

What you'll do

  • Lead programming support across multiple clinical studies to ensure timely and high-quality deliverables.
  • Coordinate programming documentation and specifications according to established company standards.
  • Communicate with study and project teams to clarify requirements and guide programmers.
  • Lead submission-ready programming deliverables for global regulatory authority filings.
  • Serve as a subject matter expert to drive department goals and key topics.
  • Guide the development of direct reports through goal-setting, coaching, and mentoring.
  • Contribute to the hiring process by screening and interviewing programming candidates.

What we're looking for

  • MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline.
  • Programming experience ( for BS holders).
  • Experience in clinical trial data within biotechnology, pharmaceutical, or health-related industries (preferred).
  • Experience in project and people management.
  • Advanced SAS programming expertise in a clinical data environment.
  • Strong understanding of clinical trial principles and regulatory submission requirements.
  • Proven ability to lead global, cross-functional teams and manage multiple concurrent projects.
  • Demonstrated mentoring or coaching experience with junior programmers.
  • Knowledge of additional programming languages such as R or Python (preferred).

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