- Company Name
- BeOne Medicines
- Job Title
- Senior Director, European Government Affairs and Public Policy - Europe
- Job Description
-
**Job title**
Senior Director, European Government Affairs and Public Policy – Europe
**Role Summary**
Lead the development and execution of a comprehensive EU government affairs and public policy strategy that promotes market access, accelerates regulatory processes, and protects intellectual property for our biopharmaceutical business. Collaborate closely with senior management, market access, corporate communications, regulatory affairs, patient advocacy, legal, and corporate affairs to align policy outcomes with corporate objectives.
**Expactations**
• Deliver a cohesive EU policy agenda that enhances access to medicines, influences regulatory reform, and safeguards IP rights.
• Maintain continuous engagement with EU institutions (Commission, Parliament, Council) and national representatives to shape public policy.
• Ensure cross‑functional alignment and prioritize initiatives that support innovation and patient access.
**Key Responsibilities**
1. Develop and implement the EU government affairs strategy in partnership with the Head of EU GAPP.
2. Monitor legislative and regulatory developments, prioritising health policy, market access, and IP matters that affect the biopharma sector.
3. Engage EU institutions, national stakeholders, and trade associations to influence favorable policy outcomes.
4. Coordinate with market access, legal, and IP teams to address compliance and potential legal challenges.
5. Integrate patient advocacy perspectives to keep access to medicines central in policy discussions.
6. Build and manage policy coalitions, deliver events, and maintain a robust external network.
7. Represent the company in trade associations and industry forums to shape collective positions on pro‑innovation policies.
8. Ensure alignment with corporate affairs for integrated national and international policy initiatives.
**Required Skills**
- Strategic policy development and execution
- Deep knowledge of EU legislative and regulatory processes
- Proven influence on EU policy and regulation (biopharma/healthcare)
- Stakeholder engagement and coalition building
- Cross‑functional collaboration (legal, regulatory, market access, communications)
- Strong analytical, communication, and presentation skills
- Project Management (MS Office, SharePoint, Smartsheet or equivalents)
- Ability to operate within a fast‑moving, global environment
**Required Education & Certifications**
- Bachelor’s degree in Public Policy, Political Science, Law, Life Sciences, or related field (advanced degree preferred).
- Professional certifications in policy or regulatory affairs are an advantage but not mandatory.