Manager, Statistical Programming - Oncology

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Location: Warren, NJ or Cambridge, MA
• Work model/flexibility: Onsite

Discover your role:

• Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables
• Lead the development and quality control of tables, listings, and graphs in support of analysis requirements
• Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests
• Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch
• 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
• Advise direct reports on procedures for data, records, and information retention
• Enjoy working with minimal supervision and taking ownership of complex deliverables
• Communicate clearly with cross-functional, multidisciplinary teams
• Think analytically and stay organized when managing multiple priorities and timelines
• Take initiative in developing deep expertise within a specialized area
• Bring a collaborative mindset to hiring, feedback, and team development
• Adapt easily to shifting priorities, including last-minute requests from senior leadership
• Approach quality and documentation with rigor in a regulated environment

This role requires:

• 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
• Strong organizational and documentation skills within a regulated environment
• Nice to have: SAS Certification

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