Senior Manager, Statistical Programming

Regeneron

Senior Manager, Statistical Programming overseeing programming support for clinical trials at Regeneron. Driving high-quality deliverables through collaboration and mentoring within a fast-growing organization.

Posted 7/28/2026full-timeWarren • Massachusetts, New Jersey • 🇺🇸 United StatesSenior💰 $150,500 - $245,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive programming expertise in clinical trial data, particularly with advanced SAS skills, while effectively leading cross-functional teams and mentoring junior programmers. Possesses a strong understanding of regulatory submission requirements and clinical trial principles.

Highest-signal resume keywords

Advanced SAS SkillsClinical Trial Data ExperienceRegulatory Submission ExpertiseCross-Functional Team LeadershipMentoring and Coaching Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Programming ExperienceClinical Trial PrinciplesRegulatory Submission RequirementsProject ManagementStatistical AnalysisData DocumentationProgramming SpecificationsGoal-SettingCoachingMentoring

Soft Skills

CollaborationAccountabilityProactive CommunicationLeadership

Industry Keywords

BiotechnologyPharmaceuticalHealth-Related IndustriesClinical Data Environment

About the role

Key responsibilities & impact

Lead programming support across multiple studies, ensuring timely, high-quality deliverables
Coordinate programming documentation and specifications, following established standards
Champion company values through excellence, collaboration, and accountability
Communicate proactively with study and project teams to clarify requirements and guide programmers
Lead submission-ready programming deliverables for global regulatory authority filings
Drive department goals and serve as a subject matter expert on key topics
Guide the development of direct reports through goal-setting, coaching, and mentoring
Contribute to hiring by screening and interviewing programming candidates

Requirements

What you’ll need

10+ years of programming experience — preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries
Advanced SAS skills honed in a clinical data environment
Strong understanding of clinical trial principles and regulatory submission requirements
Proven ability to lead global, cross-functional teams
Experience managing multiple concurrent projects and priorities
Demonstrated mentoring or coaching experience with junior programmers
MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline

Benefits

Comp & perks

annual bonuses or other incentive plans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
insurance benefits (e.g. medical, dental, vision, life and disability)
paid time off
family support benefits