Medical Director Pipeline Lead

hace 2 días


Murcia, Murcia, España Argenx A tiempo completo
About the Role

**Medical Director Pipeline, Medical Affairs EMEA**

We are seeking a highly skilled Medical Director to lead our Medical Affairs team in the EMEA region. As a key member of our global Medical Affairs organization, you will be responsible for providing medical leadership and expertise to all pipeline-related Medical Affairs activities.

Key Responsibilities
  • Develop and implement the Medical Affairs strategy for pipeline assets/indications, in partnership with Global Medical Affairs, regional medical affairs pipeline colleagues, cross-functional teams, and proportionate to enterprise priorities.
  • Develop tactical plans and activities for new pipeline indications and products, aligning with cross-functional colleagues across EMEA and global teams, including Market Access, Business Operations, and Clinical Development teams.
  • Contribute to the overall postmarketing strategy and evidence generation plans to ensure sufficient EMEA input and aligned overarching strategies.
  • Be a key member of the cross-functional EMEA pipeline strategy team, ensuring awareness, alignment, integration, and prioritization of key tactics.
  • Develop and continuously maintain the highest scientific and medical expertise across all diseases and products within the relevant therapeutic areas and be acknowledged internally and externally as an expert.
Requirements
  • Ability to develop and maintain a high level of knowledge in complex disease areas, treatments, and clinical development plans.
  • Demonstrated ability to accurately and effectively evaluate medical/scientific literature and landscape to develop effective medical affairs strategies.
  • Experience in developing, communicating, and implementing a comprehensive medical affairs plan and pre-launch plan.
  • Demonstrated ability to build productive collaborations with international medical experts.
  • Relevant experience in managing evidence generation projects.
  • Detailed understanding of regulations and practices, including related to industry interactions with healthcare professionals and product access.
  • Ability to work collaboratively and effectively together within cross-functional teams and networks.
  • Demonstrated communication skills, within a multi-cultural and multi-lingual global environment.
Preferred Qualifications
  • Medical, pharmaceutical, or high-level scientific degree (MD, PharmD preferred).
  • Minimum of 10-15 years' experience in rare diseases in Medical Affairs and clinical research and development, managing budgets and vendors.
  • European or global launch experience in rare diseases is a must.
  • Experience in new product planning is a must.
  • Business fluency in English and at least one other major European language.
What We Offer

We offer a competitive salary, extensive benefits, and the opportunity to grow and be part of a team driven by purpose, creativity, innovation, and excellence. If you are entrepreneurial, curious, and committed to making a difference for patients, then Argenx is for you.



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