Executive Director, Global Medical Affairs – Disease Area Lead, Solid Tumors

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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

• Develop, lead, and oversee the execution of gynecologic Global Medical Affairs Plan as well as future other solid tumor plans based on pipeline data advancement. • Develop and execute on a data generation strategy outside of the clinical development program, including investigator -initiated programs and real world evidence programs. • Represent Medical Affairs in early development and clinical development team meetings with a focus on contributing regional and global medical input to the clinical development plan, clinical trial design, and support successful implementation of the clinical program. • Influence and support development of disease and product specific Clinical Development strategy within thoracic cancers. • Lead with the scientific communications team on a successful Disease Area publication strategy and implement successful publication plan including review and approval of relevant abstracts and manuscripts. • Lead and work cross-functionally with Clinical Development on disease area advisory meetings. • Interpret, and present clinical trial data both internally and externally. • Partner with the Health Economics and Outcomes Research Team in providing technical and clinical expertise on relevant disease area evidence generation studies. • Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocols. • Contribute to or perform therapeutic area/indication research and competitor analysis. • Lead and execute relevant Advisory Boards. • Build and maintain strong relationships with key opinion leaders and institutions globally. • Build strong alliances and relationship with internal experts. • When appropriate be the GMA representative at Alliance partnerships. • Develop, track, execute and report on goals and objectives. • Support budget planning and management. • Be accountable for compliant business practices.

🎯 Requirements

• Advanced degree (MD, PharmD, PhD, or MD equivalent) with subspecialty training in oncology. • Extensive experience in pharma/biotech in solid tumors is required. • 8 plus years of experience within other biotech/pharmaceutical company. • Clinical solid tumor oncology experience is mandatory for this role. • Previous experience in Clinical Development in the role of medical director or clinical scientist is 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.

🏖️ Benefits

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