
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 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.
🔥 11 minutes ago
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10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 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.
• Translate, implement, and advise on global regulatory strategies • Act as a key advisor to the GRL/RRL • Lead and manage complex regulatory submissions across multiple regions • Organize and facilitate cross-functional meetings • Identify risks and propose solutions • Oversee preparation and submission of documentation • Build partnerships with senior stakeholders and cross-functional teams • Champion process optimization within the global regulatory PM function • Mentor and guide junior staff
• Bachelor’s degree in Science or related discipline; advanced degree preferred • Minimum 8+ years of experience in regulatory project management and regulatory submissions • Demonstrated experience in strategic regulatory leadership • Experience leading cross-functional and cross-regional teams • Strong business acumen, strategic thinking, and decision-making skills • Excellent verbal and written communication skills • Proficiency with project management and document management tools (e.g., Smartsheets, MS Project, Power BI, MS Office suite) • PMP or similar certification preferred
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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