Global Associate Director, Real-World Biostatistics

GSK plc

Pennsylvania

On-site

USD 150,000 - 210,000

Full time

3 days ago
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Job summary

GSK plc is seeking an Associate Director to drive value-delivery initiatives using advanced biostatistical methods and real-world data. This global role partners with cross-functional teams to shape RWE strategies for priority assets and to inform trial design, regulatory submissions, reimbursement, and safety signal assessment.

Responsibilities include leading non-interventional study design/analysis, developing robust statistical plans, and communicating results to internal and external

Qualifications

  • Ph.D. in Statistics, Data Science, Epidemiology, or related field with 6+ years of pharma/biotech experience, preferably in real-world evidence.
  • Experience with drug development processes and applying innovative statistical thinking.
  • Experience using RWD (electronic health records, claims, registries) in observational research.
  • Proficiency in R and SQL with applied observational data work.

Responsibilities

  • Lead design and analysis of non-interventional studies, ensuring methodological rigor.
  • Develop and refine statistical analysis plans and communicate findings to stakeholders.
  • Present analyses at conferences/publications and advise on regulatory submissions.
  • Contribute to RWE strategy and advanced biostatistical methods development.
  • Provide biostatistical support during regulatory interactions and guidance.

Skills

Continuing Learning
Influencing Without Authority
Leadership
Problem Solving
Statistical Methods
Statistical Programming

Education

Ph.D. in Statistics, Data Science, Epidemiology, or related field

Tools

R
SQL

Job description

GSK plc is seeking an Associate Director to drive value-delivery initiatives using advanced biostatistical methods and real-world data. This global role partners with cross-functional teams to shape RWE strategies for priority assets and to inform trial design, regulatory submissions, reimbursement, and safety signal assessment.

Responsibilities include leading non-interventional study design/analysis, developing robust statistical plans, and communicating results to internal and external

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