Associate Medical Director Neurology, Medical Affairs and Evidence Generation

Join argenxAt argenx, we build our culture from the collective power of the team and the knowledge that together, we are better. If you are entrepreneurial, curious and committed to make a difference for patients and thrive on creating solutions for rare autoimmune diseases, then argenx is for you.Next to a competitive salary with extensive benefits, we offer you the chance to grow and be a part of a team driven by purpose, creativity, innovation and science.argenxargenx is a fast-growing global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Thanks to colleagues based in Europe, the United States and Japan, we translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines. For the expansion of our Medical Affairs and Evidence Generation team, argenx is looking for an Associate Medical Director Neurology (CIDP indication) for the Developed Markets.PURPOSE OF THE FUNCTIONAs an Associate Medical Director Neurology (CIDP), you will play a pivotal role in shaping the future of healthcare by providing advanced medical and scientific expertise for the CIDP indication within the MAEG International organization. This position offers a unique opportunity to lead strategic MAEG projects, drive cross-functional collaboration, and contribute to the development and launch of innovative treatments that transform patient lives.You will act as an internal and external expert in CIDP and neurology, overseeing scientific data, clinical trials, and real-world evidence, and supporting the execution of international Medical Affairs plans. You will foster strong working relationships with cross-functional colleagues and external stakeholders, representing argenx’s values as a science-driven, patient-centric organization.ROLES AND RESPONSIBILITIESActively contribute to the development, execution and tracking of the Medical Affairs plan for CIDP for the DM region.Provide strategic medical input and oversight for key medical projects (e.g., advisory boards, medical education, scientific communication, development/review/approval of field materials, congress support, real-world evidence projects).Partner with and support country MAEG teams, as well as the Emerging and Partner Market MAEG team, to provide resources, training, and materials for excellent field execution, reporting back to the international medical and brand teams as needed.Support onboarding and continuous training programs for field medical teams, and facilitate effective systems implementation.Drive robust insight generation and facilitate analysis and internal communication of results.Develop and own dashboards, KPIs/metrics, and other relevant reports to track and communicate execution of medical activities.Provide input and tracking for budgeting and planning processes.Identify and share lessons learned and best practices across countries.Provide support for the development, review, and approval of presentation materials for scientific meetings, symposia, and other medical education activities.Provide timely medical support to clinical operations, marketing, market access, and other functions in line with local standards, regulations, and internal policies.Maintain the highest scientific and medical expertise in CIDP and neurology, including competitive environment, and be a trusted source of information internally and externally.Build valued and trusted relationships with the healthcare community through external engagement, projects, and collaborations.Ensure full adherence to compliance and ethics rules.Complete all work in accordance with regulatory requirements, industry standards, and argenx policies.SKILLS AND COMPETENCIES Demonstrated leadership in innovation, cross-functional collaboration, and shared goals.Extensive experience partnering with country medical affairs teams, cross-functional and cross-regional team and functions.Proven ability to network and partner with internal and external stakeholders.Deep understanding of complex disease areas (CIDP, neurology) and healthcare systems.Strong scientific and business acumen and the ability to interpret and communicate complex scientific dataProven track record of delivering results that meet or exceed targeted objectives.Detailed understanding of industry regulations and practices relating to Medical Affairs.Digitally savvy and proficient in medical databases and project management tools.Positive mindset and approach to meaningful quantitative and qualitative value and impact measures.Ability for frequent travel as required.Ability to work collaboratively and effectively together within cross-functional teams and networks, and with external stakeholdersDemonstrated communication skills, within a multi-cultural and multi-lingual global environmentIs agile and demonstrates adaptability, comfort with ambiguity, trust-building, and resilienceDerives energy from operating in a dynamic, complex, fast-moving, and frequently changing business environmentDemonstrable experience with project management, proactive planning and priority settingAmbitious, inquisitive naturally, a quick study, with demonstrated eagerness to continuously learn, self-improve and develop. This includes being comfortable giving and receiving feedback in a diverse environment.Passionate and prepared to lead and contribute to our culture, which is driven by our corporate values of co-creation, innovation, empowerment, excellence, and humility.EDUCATION, EXPERIENCEScientific, healthcare, or medical degree (PhD, PharmD, or MD).Significant experience in the biopharmaceutical or biotechnology industry in medical affairs (typically 6–8+ years).Experience partnering with country medical affairs teams and building out Medical Affairs capabilities.Experience working in complex disease areas and across therapeutic areas/products.Experience working with international/global functions and leadership.Experience in neurology, immunology, and/or rare diseases is an advantage.Proven knowledge of regional and country medical affairs and compliance procedures and requirements.OTHERExperience in building productive collaborations with medical experts and networks.Valid driver’s license and ability for frequent travel as required (approximately 20% - 30%).Business fluency in English and at least one other major European language.