Associate Director, Oncology Statistics — Hybrid Leadership

GlaxoSmithKline

Upper Providence (Delaware County)

Hybrid

USD 150,000 - 190,000

Full time

12 days ago

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Benefits offered by this job

Annual bonus
Healthcare
Pension plan
Shares and savings programme

Job summary

GlaxoSmithKline is seeking an Associate Director of Oncology Statistics to lead statistical planning and delivery across clinical oncology programs. You will collaborate with clinical, regulatory, safety, data science and commercial teams to shape development decisions and regulatory strategy.

You will drive methodological innovation, design robust trials, and mentor statisticians to build capability and quality within a collaborative, global environment.

Qualifications

  • Advanced degree in Statistics, Biostatistics or related quantitative discipline required.
  • Experience in oncology clinical development.
  • Experience with simulations and statistical methods using R, Python or similar tools.
  • Clear written and verbal communication skills for explaining methods and results to non-statistical colleagues.

Responsibilities

  • Provide statistical support to Oncology Projects across the pipeline.
  • Lead statistical design, analysis and interpretation for clinical programs across development phases.
  • Use simulations and advanced statistical methodology to inform trial design and risk assessment.
  • Review and contribute to statistical analysis plans, protocols and regulatory submissions.
  • Work with cross-functional teams to translate statistical insight into program strategy.
  • Mentor and coach statisticians to build capability and quality.

Skills

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

Education

MSc or higher in Statistics/Biostatistics

Tools

R
Python

Job description

GlaxoSmithKline is seeking an Associate Director of Oncology Statistics to lead statistical planning and delivery across clinical oncology programs. You will collaborate with clinical, regulatory, safety, data science and commercial teams to shape development decisions and regulatory strategy.

You will drive methodological innovation, design robust trials, and mentor statisticians to build capability and quality within a collaborative, global environment.

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