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Cluster medical director, southern europe

Madrid
Indefinido
JR Spain
Publicada el 10 septiembre
Descripción

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Cluster Medical Director, Southern Europe, Madrid Company: Mundipharma
Location: Madrid, Spain
Job Category: Other
EU work permit required: Yes
Job Reference: 57916812359316275232460
Job Views: 2
Posted: 23.07.2025
Expiry Date: 06.09.2025
Job Description: Company Description: Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.
Job Purpose: We have an exciting opportunity to join Mundipharma as the Cluster Medical Director for Southern Europe, responsible for Spain, Italy, and France (based in Spain). You will work with an interesting and varied portfolio of products across several disease areas, including a new anti-infective in severe disease launching soon. This role reports directly to the VP, Global Head of Medical Affairs, and is a key member of the Senior Medical Leadership Team, contributing to the development and implementation of Medical Affairs strategy and global transformation.
Key Responsibilities:
Provide leadership for the local Medical department, focusing on talent development and high performance culture.
Provide clinical support across Medical Affairs and the product portfolio.
Ensure Medical governance aligns with patient interests in the country.
Manage the Medical budget for the country.
Implement Global medical systems and processes locally.
Collaborate with Global Medical teams on data generation and medical communication needs.
External Engagement:
Build and maintain relationships with medical opinion leaders, experts, institutions, and societies.
Lead patient engagement activities, including advocacy groups.
Act as a medical spokesperson following communication team alignment.
Liaise with competitors to resolve disputes.
Cross-functional Support:
Provide scientific and medical expertise internally and externally.
Support Marketing initiatives and ensure compliance with regulations.
Coordinate with Regulatory Affairs, Drug Safety, R&D for seamless operations.
Oversee approval of promotional and scientific materials.
Qualifications:
Medical Doctor, PhD, or Pharmacist.
Certifications: MD, MPharm.
Experience: 8+ years in Medical Affairs, 3+ years in clinical practice.
Fluency in English (written and spoken) is mandatory.

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