
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.
10,000+ employees
Founded 2010
November 6

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.
10,000+ employees
Founded 2010
• Reporting to the Head/Director of Clinical Trial Diversity • Operationalize clinical trial diversity strategy through data-driven insights and outreach models • Collaborate across Clinical Operations, Regulatory, Development, and corporate functions • Build partnerships with sites, communities, and internal teams • Aggregate and analyze real-world data for enrollment targets • Translate strategic priorities into operational roadmaps • Serve as the analytical liaison across GCO, Regulatory, and Medical Affairs • Implement process improvements to strengthen enrollment practices
• Bachelor’s degree required; graduate degree preferred (MBA, MSc, PhD, MD, and/or MPH) • Minimum 8 years relevant clinical research experience • Demonstrated expertise in data visualization, RWD/RWE analytics, and clinical feasibility modeling • Strong understanding of FDA Diversity Action Plan requirements • Experience with clinical data warehouses and regulatory data reporting preferred • Proven ability to work independently • Must have strong soft skills with humility, kindness, and self-awareness • High attention to detail and ability to summarize complex concepts • Ability to work in a complex, fast moving, highly matrixed organization
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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