Director, Biostatistician (evergreen)

BeiGene

Remote
Base: $187,100.00 - $247,100.00 annually; bonus/eq...
Central statistical monitoring
Rbqm statistical playbook
Signal triage decision trees
Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department to support the RBQM: providing statistical design, interpretation, and governance for monitoring activities that protect subject safety, ensure data integrity, and support trial reliability across BeOne’s clinical development portfolios

Job Summary

  • Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department to support the RBQM: providing statistical design, interpretation, and governance for monitoring activities that protect subject safety, ensure data integrity, and support trial reliability across BeOne’s clinical development portfolios.
  • Accountable for development, validation, and operationalization of statistical monitoring indicators and models across one or multiple studies/programs.
  • Develop and deliver training modules for clinical monitors, safety officers, DM staff, and study teams on interpreting CSM outputs and on required actions.

Matching Summary

Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department to support the RBQM: providing statistical design, interpretation, and governance for monitoring activities that protect subject safety, ensure data integrity, and support trial reliability across BeOne’s clinical development portfolios.

Salary

Base: $187,100.00 - $247,100.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness

Skills & Requirements

Must-have

  • Central Statistical Monitoring
  • RBQM statistical playbook
  • signal triage decision trees
  • model validation and documentation
  • risk-based mindset

Nice-to-have

  • Patients First
  • Driving Excellence
  • Bold Ingenuity
  • Collaborative Spirit

Key Requirements

  • Master's degree with 7 years' experience or Ph.D with 5 years' experience
  • Demonstrated experience in clinical trial statistics RBQM/CSM
  • Strong stakeholder management and communication skills
  • Experience with model lifecycle management

Work Rights

Not specified

Tailored Resume

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