
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.
🕒 April 22
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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.
• 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 BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol • Provide scientific and medical support throughout conduct of a clinical trial • Review, query, and analyze clinical trial data • Create clinical study or program-related slide decks for internal and external use • Build and maintain opinion leader/investigator networks • Identify continuous process improvement opportunities • Support budget planning and management
• 6+ plus years of experience and success within other biotech/pharmaceutical companies • MD or DO or international equivalent degree required • Previous participation in a clinical development program is essential • Minimum 3 years relevant work experience in oncology clinical development • Experience in conducting lung Cancer clinical trials strongly preferred • 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 • Able to engage in work-related travel approximately 25% • 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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