Medical Affairs Lead Hemophilia
Listed on 2026-01-23
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Healthcare
Healthcare Management, Healthcare Administration, Healthcare Consultant
In this role
You will lead and shape the medical strategy for hemophilia in Switzerland, ensuring strong scientific engagement and high-quality medical activities. You will act as a key medical partner for internal teams and external stakeholders, translating science into value for patients. The position combines strategic leadership with hands‑on medical affairs execution.
Start Date: ASAP
Duration: Permanent
Place of Work: Basel / Remote possibilities within Switzerland
Key ResponsibilitiesLead and implement the country-level medical strategy for hemophilia in alignment with regional and global objectives
Recruit, develop and manage medical affairs team members within Switzerland
Establish and maintain strong, peer‑to‑peer scientific relationships with KOLs, medical experts and other key stakeholders
Drive scientific exchange through medical education initiatives, presentations, publications and advisory boards
Deliver high‑quality medical and scientific communication internally and externally
Support cross‑functional teams including clinical, regulatory, market access and commercial with scientific expertise
Provide medical input into local tactics and contribute to regional or global planning where relevant
Ensure medical governance, pharmacovigilance, medical information and compliance responsibilities are fulfilled
Represent medical affairs at national and international congresses, symposia and scientific meetings
Coordinate medical information requests in collaboration with global functions
Provide medical insights for business development and due diligence activities
Maintain close interaction with scientific societies, healthcare authorities, hospitals, patient organisations and NGOs
Advise leadership on medical topics and associated regulatory or legal considerations
Monitor scientific developments, guidelines and industry trends within hemophilia
Oversee clinical studies and post‑approval activities, ensuring regulatory and ethical compliance
Act as patient support program owner if applicable
University degree in medicine, life sciences or a related discipline meeting Swiss requirements
Several years of experience within the pharmaceutical or life sciences industry
Solid background in medical affairs, clinical science or related medical functions
Experience in haematology or rare diseases strongly preferred
Proven exposure to pre-launch and launch activities, strategy development and execution
Experience working within an international organisation
Strong understanding of the Swiss healthcare system, regulatory environment and decision‑making processes
Demonstrated ability to build and manage relationships with KOLs and healthcare authorities
Knowledge of pricing, access and health economics considered an advantage
Strong communication and stakeholder management skills
Fluency in German and English, French is an asset
Job
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