Regeneron
Regeneron
Regeneron is a biotechnology company that discovers, develops, and commercializes medicines for serious and underserved conditions. Its research spans allergy, cardiovascular and metabolic disease, neuroscience, oncology, hematology, ophthalmology, and rare diseases. By combining biological research with advanced technology, Regeneron works on biologics and genetic medicines designed to address complex healthcare needs. The company also highlights health equity, environmental responsibility, scientific education, and ethical corporate practices as part of its broader mission to advance patient care.

Principal Biostatistician, Oncology (Hybrid) | Regeneron

Lead statistical strategy for oncology drug development at Regeneron, from trial design and data analysis through regulatory reporting. Partner with multidisciplinary teams to guide evidence-based decisions for serious diseases.

Description

  • Translate drug development questions into statistical strategies with cross-functional teams
  • Evaluate endpoint feasibility and define appropriate analytical approaches
  • Design clinical experiments and interventional studies
  • Analyze clinical-trial and non-trial data to inform program-level decisions
  • Co-author clinical study protocols and statistical analysis plans
  • Conduct statistical analyses for interim and final reports
  • Partner with Statistical Programming on tables, figures, and listings
  • Assess software suitability and identify needs for new statistical methods or tools
  • Interpret findings and support project, management, and regulatory decisions
  • Create presentations and written reports, and present findings to management
  • Develop and deliver training for colleagues without statistical backgrounds
  • Contribute to new infrastructure and process development
  • Engage in research, professional associations, conferences, and publications
  • Collaborate with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical Scientists, Statistical Programming, Data Management, Medical Writing, and other stakeholders

Requirements

  • PhD or equivalent in statistics, biostatistics, or a related discipline with internship experience, or an MS in these fields plus more than five years of pharmaceutical-industry experience as a statistician
  • Strong ability to influence others and lead effectively
  • Proven success working across functional teams
  • Strong critical-thinking, time-management, and communication abilities
  • Thorough knowledge of statistical analysis methods and experimental and clinical-trial design
  • Expert proficiency with statistical software such as R or SAS
  • Ability to perform effectively in a fast-paced, collaborative setting
  • Willingness to travel up to 25% as needed

Benefits

  • Annual bonuses or other incentive programs
  • Equity awards
  • Pension or retirement benefits
  • 401(k) employer matching
  • Health and wellness programs
  • On-site fitness centers
  • Medical, dental, vision, life, and disability insurance
  • Paid time off
  • Family support programs
  • Reasonable recruitment-process accommodations where required

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