BeOne Medicines Ltd is seeking a Senior Director of European Government Affairs and Public Policy, responsible for shaping and executing strategies that influence regulatory frameworks and enhance market access for biopharmaceuticals across Europe. The ideal candidate will have extensive experience in government affairs within the healthcare sector, a strong understanding of EU institutions, and excellent communication skills
Job Summary
Responsible for the execution of government affairs and public policy strategies for Europe, interfacing the EU institutions.
Develop and execute a government affairs strategy for the EU advocating for policies that improve regulatory processes, promote market access, and ensure the protection of intellectual property rights.
Collaborate cross-functionally with legal and intellectual property teams to ensure compliance with regulatory and legislative frameworks, addressing potential legal challenges.
Matching Summary
Match Score: 85
BeOne Medicines Ltd is seeking a Senior Director of European Government Affairs and Public Policy, responsible for shaping and executing strategies that influence regulatory frameworks and enhance market access for biopharmaceuticals across Europe. The ideal candidate will have extensive experience in government affairs within the healthcare sector, a strong understanding of EU institutions, and excellent communication skills.
Salary
Base: 194,400.00 EUR - 243,000.00 EUR; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
EU institutions engagement
Policy development and execution
Market access advocacy
Intellectual property protection
Cross-functional collaboration
Nice-to-have
Scientific and business acumen
Passion for fighting cancer
Collaborative spirit
Proactive stakeholder engagement
Key Requirements
12+ years of experience in government affairs, public policy, or related fields
Extensive knowledge of the life science business model
Extensive experience working with government institutions at European level
Proven track record in influencing policy and regulatory frameworks in the EU
Deep knowledge of European biopharmaceutical regulatory and policy environments
Fluency in English; proficiency in French and an additional European language is a plus