Lead Statistical Programming Manager

Regeneron

New Jersey

On-site

USD 129,000 - 210,000

Full time

30 hours ago
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Job summary

Regeneron seeks a Manager, Statistical Programming to lead programming deliverables for a study from start to regulatory submission and launch. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and reporting across the portfolio.

This role requires a Master’s degree with 8–10 years of relevant experience, or a related field with 5+ years in programming, including project and people management.

Qualifications

  • Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)
  • Proven experience leading programming deliverables within a clinical study team
  • Experience providing input on hiring, feedback, and performance evaluation

Responsibilities

  • Lead programming deliverables from a single study through regulatory approval, product launch, and annual reports
  • Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests
  • Serve as programming representative on a multidisciplinary study team
  • Partner with management to determine resource requirements for your therapeutic area or department
  • Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles
  • Provide feedback to management on team members' contributions to support performance evaluations and goal-setting

Skills

Leadership
Cross-functional collaboration
Programming oversight
Communication
Analytical thinking

Education

Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline

Tools

SAS

Job description

Regeneron seeks a Manager, Statistical Programming to lead programming deliverables for a study from start to regulatory submission and launch. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and reporting across the portfolio.

This role requires a Master’s degree with 8–10 years of relevant experience, or a related field with 5+ years in programming, including project and people management.

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