Director, Central Statistical Monitoring

BeOne Medicines

Base: $187,100.00 - $247,100.00 annually; bonus/eq...
Not specified
Central statistical monitoring experience
Statistical risk indicator development
Anomaly detection model validation
BeOne Medicines is seeking a Director of Central Statistical Monitoring to lead their CSM team, focusing on statistical design and governance for clinical trials aimed at enhancing patient safety and data integrity. The ideal candidate will possess strong experience in clinical trial statistics, risk-based quality management, and effective stakeholder communication

Job Summary

  • The role involves leading the Central Statistical Monitoring team to protect subject safety and ensure data integrity across BeOne's clinical development portfolios.
  • Candidates will be accountable for developing statistical monitoring indicators, validating models, and defining signal characterization methods in collaboration with governance bodies.
  • BeOne offers a comprehensive benefits package including medical, dental, vision, 401(k), life insurance, paid time off, and opportunities for discretionary equity awards.

Matching Summary

Match Score: 85

BeOne Medicines is seeking a Director of Central Statistical Monitoring to lead their CSM team, focusing on statistical design and governance for clinical trials aimed at enhancing patient safety and data integrity. The ideal candidate will possess strong experience in clinical trial statistics, risk-based quality management, and effective stakeholder communication.

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, Wellness

Skills & Requirements

Must-have

  • Central Statistical Monitoring experience
  • Statistical risk indicator development
  • Anomaly detection model validation
  • Signal triage decision logic
  • RBQM playbook implementation

Nice-to-have

  • Cross-functional stakeholder management
  • Risk-based quality mindset
  • Training material development
  • Continuous improvement focus

Key Requirements

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

Work Rights

Not specified

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