
10,000+ employees
Founded 2010
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.
🕒 March 4
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10,000+ employees
Founded 2010
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.
• Support BeOne Clinical and Medical Hematology assets by successful execution of clinical development programs and deliverables in partnership across the organization • Involved in clinical program strategy and help assure that activities are executed within expected scope, budget and timelines • Work closely with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance, regulatory, molecular diagnostics, and translational research • Facilitate generation of, author, update, and/or review key documents • Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies • Provide scientific expertise for selection of investigator and vendors • Train colleagues, CRO staff, and study site staff • Provide scientific and medical support throughout conduct of a clinical trial • Review, query, and analyze clinical trial data • Interpret, and present clinical trial data both internally and externally • Represent a clinical study or development program on one or more teams or sub teams • Create clinical study or program-related slide decks for internal and external use • Build and maintain opinion leader/investigator networks
• 6 plus years of experience within other biotech/pharmaceutical or relevant academic credentials companies • Advanced degree (MD or MD equivalent) with subspecialty training in hematology/oncology (preferred) • Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report) • Clinical oncology experience: candidates with exceptional experience in other therapeutic areas would be considered if they demonstrated clear potential to apply their existing skills to oncology • Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing • High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills • Knowledge of GCP and ICH Guidelines • Flexibility to work with colleagues in a global setting • Strategic leader with demonstrated success building, managing and developing individuals and teams is preferred • Experience with the development and support of related SOPs and policies is expected • Knowledge of industry standard Clinical Development IT solutions expected
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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