Director, Central Statistical Monitoring

BeOne Medicines Ltd

Remote
$187,100.00 - $247,100.00 annually py
Remote
Statistical design and interpretation
Develop and validate statistical models
Signal detection and characterization
BeOne Medicines Ltd is seeking a Director of Central Statistical Monitoring to lead its Global Statistics department, focusing on risk-based quality management in clinical trials. The ideal candidate should have significant experience in clinical trial statistics, strong stakeholder management skills, and the ability to develop and validate statistical monitoring tools

Job Summary

  • Lead the Central Statistical Monitoring (CSM) team to support RBQM, providing statistical design, interpretation, and governance for monitoring activities.
  • Accountable for the development, validation, and operationalization of statistical monitoring indicators and models across clinical development portfolios.
  • Develop and deliver training modules for clinical monitors, safety officers, DM staff, and study teams on interpreting CSM outputs and required actions.

Matching Summary

Match Score: 85

BeOne Medicines Ltd is seeking a Director of Central Statistical Monitoring to lead its Global Statistics department, focusing on risk-based quality management in clinical trials. The ideal candidate should have significant experience in clinical trial statistics, strong stakeholder management skills, and the ability to develop and validate statistical monitoring tools.

Salary

$187,100.00 - $247,100.00 annually

Skills & Requirements

Must-have

  • statistical design and interpretation
  • develop and validate statistical models
  • signal detection and characterization
  • cross-functional interpretation and communication
  • operationalization of decision logic
  • training and stakeholder enablement

Nice-to-have

  • scientific and business professionals
  • highly motivated and collaborative
  • passionate interest in fighting cancer
  • risk-based mindset
  • continuous improvement

Key Requirements

  • Master's degree with 7 years' experience or Ph.D with 5 years' experience
  • Demonstrated experience in clinical trial statistics
  • RBQM/CSM and signal triage experience
  • Model lifecycle management, validation, and documentation experience

Work Rights

Not specified

Tailored Resume

Cover Letter