Manager Statistical Programming

Regeneron

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Warren, NJCambridge, MA
Salary
$128,600–$210,000 / yr
Employment
Full-time
Posted
53 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $185k
This role $169k
$118k most similar roles pay here $231k

This role pays less than 65% of similar roles. Most pay $159,000–$211,200 — the shaded band above. At the midpoint, this role pays about $169k 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 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 · Manager Statistical Programming

Manager Statistical Programming joins the Statistical Programming team to support a study team across the clinical portfolio. This role involves leading programming deliverables from a single study through regulatory approval, product launch, and annual reports while collaborating with cross-functional colleagues and CROs to ensure high-quality analysis. The manager will lead the development and quality control of tables, listings, and graphs, manage complex ad hoc requests, and serve as the programming representative on multidisciplinary teams. Key responsibilities include determining resource requirements, participating in hiring and performance evaluations, and advising direct reports on data retention procedures. Candidates should possess a Master's degree in a relevant field like Statistics or Computer Science and have experience with clinical study programming. A SAS Certification is considered a preferred qualification for this role within the regulated pharmaceutical environment.

What you'll do

  • Lead programming deliverables from initial study through regulatory approval, product launch, and annual reporting.
  • Manage the development and quality control of tables, listings, and graphs for analysis requirements.
  • Track progress and completion of all programming deliverables, including complex ad hoc requests.
  • Serve as the primary programming representative on multidisciplinary study teams to ensure timely support.
  • Partner with management to determine resource requirements for specific therapeutic areas or departments.
  • Participate in the hiring process by reviewing resumes and screening candidates for contractor and permanent roles.
  • Provide feedback to management regarding team member performance and contributions for evaluations.
  • Advise direct reports on procedures for data, records, and information retention.

What we're looking for

  • Master's degree with 8-10 years of relevant work experience.
  • Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with 5+ years of programming and management experience.
  • Proven experience leading programming deliverables within a clinical study team.
  • Experience providing input on hiring, feedback, and performance evaluation.
  • Strong organizational and documentation skills within a regulated environment.
  • SAS Certification (preferred).

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