Associate Director, Central Statistical Monitoring

BeOne Medicines

Base: $162,600.00 - $212,600.00 annually; bonus/eq...
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Central statistical monitoring expertise
Risk-based quality management experience
Statistical model validation skills
** BeOne Medicines is seeking an Associate Director for their Central Statistical Monitoring team, responsible for leading statistical design and monitoring to ensure data integrity in clinical trials. The ideal candidate should possess strong expertise in biostatistics, particularly in risk-based quality management and signal triage, along with excellent communication skills. **

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 responsible for developing statistical risk indicators, validating algorithms, and defining decision trees for signal investigation workflows.
  • BeOne offers a comprehensive benefits package including medical, dental, vision, 401(k), and opportunities for equity awards and annual bonuses.

Matching Summary

Match Score: 75

** BeOne Medicines is seeking an Associate Director for their Central Statistical Monitoring team, responsible for leading statistical design and monitoring to ensure data integrity in clinical trials. The ideal candidate should possess strong expertise in biostatistics, particularly in risk-based quality management and signal triage, along with excellent communication skills. **

Salary

Base: $162,600.00 - $212,600.00 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

Skills & Requirements

Must-have

  • Central Statistical Monitoring expertise
  • Risk-Based Quality Management experience
  • Statistical model validation skills
  • Clinical trial statistics background
  • Signal triage and characterization

Nice-to-have

  • Strong stakeholder management skills
  • Experience with PowerBI dashboards
  • Ability to promote risk-based mindset
  • Collaborative spirit across teams
  • Training delivery capabilities

Key Requirements

  • Master's degree in biostatistics or related field
  • 6 years of experience in clinical trial statistics
  • Ph.D. with 4 years of relevant experience
  • Demonstrated RBQM and CSM experience
  • Model lifecycle management and validation experience

Work Rights

Not specified

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