
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 19

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
• The Head of Global Clinical Process Management is responsible for designing, implementing, and optimizing processes across multiple locations or regions. • Analyze existing processes, identify areas for improvement, and implement changes to enhance efficiency and quality. • Collaborate with various teams cross functionally and partner with all functions across Clinical Development and Global Process Owners (GPOs). • Shape and execute a continuous improvement plan for end-to-end clinical trial processes owned by Global Clinical Operations. • Monitor, study management, identifying areas for improvement, designing and implementing process improvements, and leading process improvement teams. • Assess, plan, and implement global processes, strategies, and solutions for Clinical Operations.
• Bachelor’s Degree with minimum of 12+ years of experience in pharmaceutical or biotechnology drug development • Mid/large pharma experience (preferably clinical operations, process, quality, or compliance roles) • ICH GCP subject matter expert • Knowledgeable of regulatory requirements (e.g., FDA, MHRA/EMA) • Experience working in a cross-functional, global environment • Strong written and verbal communication skills • Deep experience and expertise in end-to-end clinical trial processes including experience in one or more key functions (e.g., clinical research, clinical operations, data management, biostatistics, project management) • Strong leadership, collaboration, and influencing skills in a complex, matrix environment including team leadership or project management • Experience in clinical trial process design, harmonization/optimization, and implementation • Understanding of industry trends (e.g., regulatory, technology) with ability to apply them to process improvement • Six Sigma certification and/or experience with process mapping tools (e.g., Visio, Power Point) desirable.
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
Apply NowNovember 19
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