Senior Manager, Statistical Programming - Internal Medicine

Regeneron Pharmaceuticals, Inc; Cambourne; On-site; GBP 105,000 - 143,000; Full time

Benefits offered by this job

SAS Certification

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Senior Manager, Statistical Programming to lead analysis programming across clinical studies.

You will oversee deliverables from single studies through regulatory approval, collaborating with study teams, CROs, and colleagues to shape programming standards. The role emphasizes mentoring, development of data models and reusable processes, and ensuring timely, high quality support for submissions and launches, while adapting to shifting priorities and

Qualifications

• Master's degree or BS with substantial experience in a relevant field.

Responsibilities

• Coordinate and oversee analysis programming within your therapeutic area, tracking progress and completion of deliverables.
• Manage and coordinate programming and quality control of analysis datasets and outputs in support of regulatory submissions.
• Mentor others on the use of standardization tools and therapeutic area standard analysis approaches.
• Serve as the programming representative on a multidisciplinary study team, ensuring timely, quality support through regulatory approval and launch.
• Develop data models, programming standards, and code, and train end users on project standards.
• Mentor junior staff, fostering a collaborative environment and modeling strong team behavior.
• Contribute to programming development and quality control using established tools and methodologies.
• Advise team members on procedures for data, records, and information retention.
• Enjoy leading programming work independently while staying closely connected to a broader project team.
• Think in terms of standards, consistency, and reusable processes across studies.
• Communicate clearly with cross-functional and multidisciplinary stakeholders.
• Take pride in mentoring and developing less experienced colleagues.
• Stay organized and detail-oriented when managing multiple deliverables and timelines.
• Approach quality control with rigor and a genuine sense of ownership.
• Adapt comfortably to shifting priorities, including ad hoc requests from senior leadership

Skills

Programming leadership

Mentoring

Cross-functional collaboration

Regulatory submissions support

SAS programming

Education

Master's degree in a relevant field

Tools

SAS

Job description

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 Senior Manager, Statistical Programming to join our Statistical Programming team, supporting a therapeutic area across our clinical portfolio. In this role, you will provide programming leadership on project teams, overseeing deliverables from single studies through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and departmental colleagues to shape and implement programming standards.

When & where:

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

Discover your role:

• Coordinate and oversee analysis programming within your therapeutic area, tracking progress and completion of deliverables
• Manage and coordinate programming and quality control of analysis datasets and outputs in support of regulatory submissions
• Mentor others on the use of standardization tools and therapeutic area standard analysis approaches
• Serve as the programming representative on a multidisciplinary study team, ensuring timely, quality support through regulatory approval and launch
• Develop data models, programming standards, and code, and train end users on project standards
• Mentor junior staff, fostering a collaborative environment and modeling strong team behavior
• Contribute to programming development and quality control using established tools and methodologies
• Advise team members on procedures for data, records, and information retention
• Enjoy leading programming work independently while staying closely connected to a broader project team
• Think in terms of standards, consistency, and reusable processes across studies
• Communicate clearly with cross-functional and multidisciplinary stakeholders
• Take pride in mentoring and developing less experienced colleagues
• Stay organized and detail-oriented when managing multiple deliverables and timelines
• Approach quality control with rigor and a genuine sense of ownership
• Adapt comfortably to shifting priorities, including ad hoc requests from senior leadership

This role requires:

• Master's degree with 10+ (or BS 12+) years of relevant experience
• Proven experience leading programming deliverables within a clinical or therapeutic area
• Strong mentoring and team collaboration skills
• Experience developing and applying programming standards and data models
• Nice to haves: SAS Certification

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