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Regeneron

Senior Manager, Statistical Programming – Hematology

Regeneron

. Lead programming support across multiple studies, ensuring timely, high-quality deliverables .

Posted 10/9/2026full-timeUnited StatesSenior💰 $150,500 - $245,500 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates advanced SAS programming expertise in clinical data environments, with a strong understanding of clinical trial principles and regulatory submission requirements. Proven ability to lead global, cross-functional teams while mentoring junior programmers and managing multiple projects.

Highest-signal resume keywords
Advanced SAS ProgrammingClinical Trial PrinciplesRegulatory Submission RequirementsProject ManagementMentoring and Coaching

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Programming ExperienceStatistical AnalysisData ManagementR ProgrammingPython Programming
Soft Skills
LeadershipCommunicationCollaborationCoachingGoal-Setting
Industry Keywords
BiotechnologyPharmaceuticalHealth-Related IndustriesClinical Trial DataGlobal Regulatory Authority Filings

Tech Stack

Tools & technologies
Python

About the role

Key responsibilities & impact
  • Lead programming support across multiple studies, ensuring timely, high-quality deliverables
  • Coordinate programming documentation and specifications according to established standards
  • Communicate 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 direct reports through goal-setting, coaching, and mentoring
  • Contribute to hiring by screening and interviewing programming candidates
  • Provide technical leadership across project teams within one or more therapeutic areas
  • Drive programming deliverables from single studies through regulatory approval, product launch, and beyond
  • Collaborate with partnering functions, external service providers, and study teams

Requirements

What you’ll need
  • MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline
  • 10+ years of programming experience, or 12+ years for BS
  • Programming experience preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries
  • Some project and people management experience
  • Advanced SAS programming expertise 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
  • Knowledge of additional programming languages such as R or Python is preferred

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
  • medical, dental, vision, life and disability insurance benefits
  • paid time off
  • family support benefits
  • reasonable accommodation during the recruitment process where required