Senior Manager, Statistical Programming — Lead Global Trials

BioSpace; New Jersey; Hybrid; USD 150,500 - 245,500; Full time

Job summary

Regeneron is seeking a Senior Manager, Statistical Programming to provide technical leadership across project teams in a fast-growing, science-driven organization. Based in Warren, NJ or Cambridge, MA, this hybrid-on-site role drives high-quality programming deliverables from studies through regulatory approval and product launch.

You will lead programming across multiple studies, coordinate documentation, mentor staff, and support global regulatory submissions while collaborating with external

Qualifications

• Advanced SAS programming in a clinical data environment.
• Understanding of clinical trial principles and regulatory submission requirements.
• Experience leading global cross-functional teams.
• Mentoring or coaching of junior programmers.
• Education: MS or BS in relevant field; 10+ years programming experience (12+ for BS).

Responsibilities

• Lead programming support across multiple studies, ensuring timely, high-quality deliverables
• Coordinate programming documentation and specifications, following established standards
• Communicate proactively with study and project teams to clarify requirements and guide programmers
• Lead submission-ready programming deliverables for global regulatory authority filings
• Guide the development of direct reports through goal-setting, coaching, and mentoring
• Contribute to hiring by screening and interviewing programming candidates

Skills

Advanced SAS programming

Clinical data experience

Cross-functional collaboration

Regulatory submissions

Mentoring

Education

MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline

Tools

R

Python

Job description

Regeneron is seeking a Senior Manager, Statistical Programming to provide technical leadership across project teams in a fast-growing, science-driven organization. Based in Warren, NJ or Cambridge, MA, this hybrid-on-site role drives high-quality programming deliverables from studies through regulatory approval and product launch.

You will lead programming across multiple studies, coordinate documentation, mentor staff, and support global regulatory submissions while collaborating with external