BeOne Medicines
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.
Medical Director, Hematology
🕒 June 11
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BeOne Medicines
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.
📋 Description
• Support BeOne clinical assets and pipeline by executing clinical development programs • Facilitate generation of, author, update, and/or review key documents • Partner with clinical operations and other functional areas for successful implementation and execution of clinical studies • Provide scientific expertise for selection of investigator and vendors • Train BeOne colleagues and study site staff on the therapeutic area, molecule, and/or clinical protocol • Provide scientific and medical support throughout the conduct of clinical trials • Review, query, and analyze clinical trial data • Build and maintain opinion leader/investigator networks
🎯 Requirements
• MD (or equivalent medical degree); board certification or eligibility in relevant therapeutic area (e.g., oncology, hematology) • Clinical training with experience in drug development or clinical research, ideally across Phases I–III • Strong understanding of clinical trial design, GCP and regulatory environment for submissions (IND, CTA, NDA, BLA) • Demonstrated safety oversight skills, familiarity with DSURs, PSURs, and safety committees • Excellent communication skills, capable of engaging internal teams, external partners, and regulators.
🏖️ Benefits
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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