Manager Statistical Programming

Regeneron

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Cambridge, MAWarren, NJ
Salary
$128,600–$210,000 / yr
Employment
Full-time
Posted
61 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $186k
This role $169k
$118k most similar roles pay here $231k

This role pays less than 68% of similar roles. Most pay $160,400–$211,200 — the shaded band above. At the midpoint, this role pays about $169k versus about $186k 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 42 open roles on FindRole.

Listed pay typically runs $128,600–$219,200 across 32 roles with salary data.

Most-posted roles

View all roles at Regeneron

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 oversee 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 strong organizational skills and experience in a regulated environment. Required qualifications include a Master's degree in a relevant field like Statistics or Computer Science, with extensive experience in clinical study programming and team management. SAS Certification is considered a preferred asset.

What you'll do

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

What we're looking for

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

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