BeOne Medicines
10,000+ employees
Founded 2010
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
Associate Director, Biostatistics – Central Statistical Monitoring
🕒 January 14
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BeOne Medicines
10,000+ employees
Founded 2010
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
📋 Description
• Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department • Provide statistical design, interpretation, and governance for monitoring activities • Develop, validate, and operationalize statistical monitoring indicators and models • Act as the CSM statistician interfacing with clinical study statisticians and other stakeholders • Collaborate with governance bodies to define statistical thresholds and signal characterization methods • Produce tiered deliverables for various stakeholders • Develop and deliver training modules for clinical monitors, safety officers, and study teams • Define KPIs for CSM effectiveness and monitor performance dashboards
🎯 Requirements
• Master's degree with 6 years' experience or Ph.D with 4 years' experience in biostatistics/statistics or related quantitative field • Demonstrated experience in clinical trial statistics RBQM/CSM, and signal triage • Strong stakeholder management and communication skills • Experience with model lifecycle management, validation, and documentation for audits/inspections • Computer Skills: Microsoft Office, PowerBI
🏖️ Benefits
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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