BeOne Medicines
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
đź’Š Pharmaceuticals
Biotechnology • Healthcare • Pharmaceuticals
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 the 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.
Director, Process Optimization Lead
đź•’ July 30
🇺🇸 United States – Remote
đź’µ $171.9k - $231.9k / year
⏰ Full Time
đźź Senior
đź‘” Director
đź‘» Ghost score 1%
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BeOne Medicines
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
đź’Š Pharmaceuticals
Biotechnology • Healthcare • Pharmaceuticals
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 the 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.
đź“‹ Description
• Responsible for the business operations of the Program and Study Management (P&SM) function • Driving operational excellence, innovation, and continuous process improvement • Identifying process optimization opportunities to enhance team working efficiency • Collaborating with the P&SM team, other GCO functional teams, and cross-functional teams on process optimization and strategy alignment • Inspiring and leading initiatives to enhance the necessary technical skills and competencies within the Global Clinical Study Management team
🎯 Requirements
• Bachelor or higher degrees (life science preferred, including medicine, nursing, biology, and laboratory technology) • Fluent in written and verbal English • 10 years or above in clinical or drug development in the biotech/pharmaceutical/CRO industry or the relevant clinical research field • Minimum of 8 years of project management and/or clinical monitoring/ or start-up experience
🏖️ Benefits
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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