Associate Director, Central Statistical Monitoring

BeOne Medicines

Remote
$162,600.00 - $212,600.00 annually; annual bonus p...
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Statistical design and interpretation
Monitoring indicators and models
Signal detection and characterization
** BeOne Medicines is seeking an Associate Director of Central Statistical Monitoring to lead their CSM team in enhancing clinical trial safety and data integrity. This remote position requires a strong background in biostatistics and experience in clinical trial statistics, with responsibilities including statistical design, signal detection, and cross-functional communication. **

Job Summary

  • Lead the Central Statistical Monitoring (CSM) team to support RBQM, providing statistical design, interpretation, and governance for monitoring activities.
  • Accountable for development, validation, and operationalization of statistical monitoring indicators and models across studies/programs.
  • 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: 75

** BeOne Medicines is seeking an Associate Director of Central Statistical Monitoring to lead their CSM team in enhancing clinical trial safety and data integrity. This remote position requires a strong background in biostatistics and experience in clinical trial statistics, with responsibilities including statistical design, signal detection, and cross-functional communication. **

Salary

$162,600.00 - $212,600.00 annually; Annual bonus plan and equity awards; Comprehensive benefits package

Skills & Requirements

Must-have

  • statistical design and interpretation
  • monitoring indicators and models
  • signal detection and characterization
  • cross-functional interpretation and communication
  • risk-based quality management (RBQM)

Nice-to-have

  • highly motivated, collaborative, passionate
  • change agent for risk-based mindset
  • training for cross-functional stakeholders

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
  • Experience with model lifecycle management, validation, and documentation

Work Rights

Not specified

Tailored Resume

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