Lead Statistical Programming Manager

Regeneron Pharmaceuticals, Inc; New Jersey; On-site; USD 129,000 - 210,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc is seeking a Manager, Statistical Programming to lead deliverables from a single study through regulatory approval, product launch, and annual reports. You will manage programming efforts, develop and QC tables/graphs, and collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis.

The role emphasizes ownership, rigorous documentation, and adaptability in a regulated, onsite environment at Warren, NJ or Cambridge, MA

Qualifications

• Master's degree with 8–10 years of relevant work experience (or a Master’s degree with 5+ years plus 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

Responsibilities

• Lead programming deliverables from a single study through regulatory approval and launch
• Develop and quality control tables, listings, and graphs for analysis
• Manage programming effort, tracking progress and completing deliverables
• Serve as programming representative on a multidisciplinary study team and collaborate with CROs and cross-functional colleagues
• Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles
• Advise on procedures for data retention and documentation

Skills

Project management

People management

Regulated environment

Documentation

Education

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

Tools

SAS

Job description

Regeneron Pharmaceuticals, Inc is seeking a Manager, Statistical Programming to lead deliverables from a single study through regulatory approval, product launch, and annual reports. You will manage programming efforts, develop and QC tables/graphs, and collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis.

The role emphasizes ownership, rigorous documentation, and adaptability in a regulated, onsite environment at Warren, NJ or Cambridge, MA