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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.
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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
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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.
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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