VP US Medical Affairs and Evidence Generation
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About The Position
Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. Argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases. We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients. The Vice President of US Medical Affairs and Evidence Generation, US is responsible for overseeing the strategic and operational activities of the Medical Affairs and Evidence Generation Community. This role ensures that medical and evidence generation strategies align with the company's objectives, driving scientific excellence and supporting the successful development, launch, and commercialization of biotechnology products. Key responsibilities include developing and implementing medical strategies that support the overall business objectives, collaborating with Global Medical Affairs and leadership to integrate medical insights into strategic planning, and identifying data gaps while designing research projects. The VP will drive innovation in medical affairs to enhance patient outcomes and product success for our vision for argenx 2030. Additionally, this role involves providing US medical perspective and insights to the broader organization, designing and ensuring a strong US KOL relationship strategy, and representing the company at medical conferences, symposia, and meetings with key opinion leaders (KOLs). The VP will also ensure effective communication of scientific data to internal and external stakeholders, oversee interactions with US regulatory agencies regarding medical and scientific issues, and maintain up-to-date knowledge of relevant regulations and industry standards. Working closely with R&D, commercial, regulatory, and other departments, the VP will ensure alignment and integration of medical strategies for the US, support the marketing team with medical insights and data, and collaborate with market access and health economics and outcomes research teams to support reimbursement strategies. Finally, the VP will lead, mentor, and develop a high-performing US Medical Affairs Community, fostering a culture of scientific excellence, innovation, and continuous improvement while managing departmental budgets and resources effectively.
