Associate Director, Central Statistical Monitoring

BeOne Medicines Ltd

Remote
$162,600.00 - $212,600.00 annually; not specified;...
Remote
Central statistical monitoring (csm)
Risk-based quality management (rbqm)
Statistical design and interpretation
BeOne Medicines Ltd is seeking an Associate Director for Central Statistical Monitoring, responsible for leading a team that supports risk-based quality management in clinical trials. The ideal candidate will possess a strong background in biostatistics, clinical trial statistics, and effective stakeholder communication, all while sharing a passion for fighting cancer

Job Summary

  • Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department to support RBQM, providing statistical design, interpretation, and governance for monitoring activities that protect subject safety, ensure data integrity, and support trial reliability.
  • Accountable for development, validation, and operationalization of statistical monitoring indicators and models across one or multiple studies/programs, interfacing with various clinical and operational teams.
  • Develop and deliver training modules for clinical monitors, safety officers, DM staff, and study teams on interpreting CSM outputs and on required actions, while acting as a change agent to promote a risk-based mindset.

Matching Summary

Match Score: 85

BeOne Medicines Ltd is seeking an Associate Director for Central Statistical Monitoring, responsible for leading a team that supports risk-based quality management in clinical trials. The ideal candidate will possess a strong background in biostatistics, clinical trial statistics, and effective stakeholder communication, all while sharing a passion for fighting cancer.

Salary

$162,600.00 - $212,600.00 annually; Not specified; Comprehensive benefits package

Skills & Requirements

Must-have

  • Central Statistical Monitoring (CSM)
  • Risk-Based Quality Management (RBQM)
  • statistical design and interpretation
  • signal detection and characterization
  • model validation and documentation
  • cross-functional communication

Nice-to-have

  • scientific and business professionals
  • highly motivated and collaborative
  • passionate interest in fighting cancer
  • change agent for risk-based mindset

Key Requirements

  • Master's degree with 6 years' experience or Ph.D with 4 years' experience
  • Demonstrated experience in clinical trial statistics
  • RBQM/CSM and signal triage experience
  • Strong stakeholder management and communication skills
  • Experience with model lifecycle management, validation, and documentation

Work Rights

Not specified

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