Statistical Programming Lead - Clinical Studies & Regulatory

Regeneron Pharmaceuticals; Cambridge; On-site; GBP 96,000 - 157,000; Full time

Job summary

Regeneron Pharmaceuticals is seeking a Manager, Statistical Programming to lead programming deliverables for a study through regulatory approval, launch, and annual reports. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high‑quality analysis and reporting.

The role requires a Master’s degree with 6+ years (or a BS with 7+ years) in a relevant field, and experience guiding deliverables in a regulated environment.

Qualifications

• Master’s degree with 6+ years (or BS 7+) of relevant work 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

Responsibilities

• Lead programming deliverables from a single study through regulatory approval and launch.
• Develop and quality control tables, listings, and graphs for analysis requirements.
• Manage programming effort, tracking progress and ad hoc requests.
• Serve as programming representative on multidisciplinary study teams.
• Partner with management to determine resource requirements.
• Contribute to hiring by screening resumes for contractor and permanent roles.
• Provide feedback on team contributions for performance evaluations.
• Advise on data retention procedures.
• Communicate clearly with cross-functional teams and manage priorities.
• Adapt to shifting priorities and tight timelines.
• Approach quality and documentation rigor in regulated environment.

Skills

Leading programming deliverables

Clinical study team experience

Hiring feedback & performance input

Regulated documentation

Education

Master’s degree or BS in related field

Tools

SAS Certification

Job description

Regeneron Pharmaceuticals is seeking a Manager, Statistical Programming to lead programming deliverables for a study through regulatory approval, launch, and annual reports. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high‑quality analysis and reporting.

The role requires a Master’s degree with 6+ years (or a BS with 7+ years) in a relevant field, and experience guiding deliverables in a regulated environment.