
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.
🕒 June 5
Improve your chances of getting an interview by checking your resume score before you apply.

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 assets by successful execution of clinical development programs • Jointly develop clinical program strategy and assure execution within expected scope, budget, and timelines • Facilitate generation of, author, update, and review key documents • Partner with clinical operations and other functional areas for successful implementation of clinical studies • Provide scientific expertise for selection of investigator and vendors • Train BeOne colleagues, CRO staff, and study site staff • Provide scientific and medical support during clinical trials • Review, query, and analyze clinical trial data • Interpret and present clinical trial data • Create and present clinical study or program-related slide decks • Build and maintain opinion leader/investigator networks
• 5 plus years of experience in biotech/pharmaceutical companies • MD or foreign equivalent • Previous participation in clinical development programs across all stages of clinical trials • Clinical oncology experience preferred but exceptional experience in other therapeutic areas may be considered • Expert understanding of global clinical study design and drug development process • High level of communication (written and verbal) and interpersonal skills • Knowledge of GCP and ICH Guidelines • Flexibility to work with colleagues in a global setting • Ability to engage in work-related travel approximately 25% • Experience with development and support of related SOPs and policies • Knowledge of industry-standard Clinical Development IT solutions
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness • Annual bonus plan • Incentive compensation plan • Equity awards • Employee Stock Purchase Plan
Apply Now🕒 June 5
Senior Director at Huron guiding healthcare organizations in business transformation and operational improvements. Leading diverse teams to drive innovation and optimize client success in the industry.
🕒 June 5
Facility Design Senior Director leading facility design projects in the US Foods Supply Chain. Ensuring compliance with operational, safety, and regulatory standards.
🕒 June 5
Senior technology leader managing enterprise applications and global IT functions at Telix Pharmaceuticals. Driving operational excellence, compliance, and alignment with business priorities.
🕒 June 4
Associate Director, CMC Statistician providing statistical leadership for specification setting at Vaxcyte. Collaborating with cross-functional teams to develop statistically sound approaches in vaccine development.
🕒 June 4
Senior Scientific Director overseeing scientific content development for assigned accounts in medical education. Collaborating with clients and leading strategic initiatives in pharmaceutical communications.