Director Clinical Development – Solid Tumors, GI

🕒 April 15

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BeOne Medicines

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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.

📋 Description

• Support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners • Jointly develop clinical program strategy and help assure that activities are executed within expected scope, budget and timelines • Play a key role in the establishment and growth of Clinical Research functions • 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 • Interpret, and present clinical trial data both internally and externally • Build and maintain opinion leader/investigator networks • Identify continuous process improvement opportunities • Develop, track, execute and report on goals and objectives • Support budget planning and management

🎯 Requirements

• MD or DO or international equivalent degree required • 5 plus years of experience and success within other biotech/pharmaceutical companies • 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 • 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

🏖️ Benefits

• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness