Associate Director, Central Statistical Monitoring

BeiGene

Remote
$162,600.00 - $212,600.00 annually; annual bonus p...
Remote
Statistical monitoring indicators and models
Signal detection and characterization
Cross-functional interpretation and communication
BeiGene is seeking an Associate Director of Central Statistical Monitoring to lead the CSM team in their Global Statistics department, focusing on risk-based quality management in clinical trials. The ideal candidate will have a strong background in biostatistics, experience with clinical trial statistics, and excellent stakeholder management skills

Job Summary

  • Lead the Central Statistical Monitoring (CSM) team 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, interfacing with various clinical and operational teams to ensure signals are interpretable and actionable.
  • Develop and deliver training modules on interpreting CSM outputs and provide statistical support during audits/inspections, acting as a change agent to promote a risk-based mindset.

Matching Summary

Match Score: 85

BeiGene is seeking an Associate Director of Central Statistical Monitoring to lead the CSM team in their Global Statistics department, focusing on risk-based quality management in clinical trials. The ideal candidate will have a strong background in biostatistics, experience with clinical trial statistics, and excellent stakeholder management skills.

Salary

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

Skills & Requirements

Must-have

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

Nice-to-have

  • scientific and business professionals
  • highly motivated, 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

Tailored Resume

Cover Letter