Medical Information Director – Customer Management

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. Argenx is a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases and cancer. Partnering with leading academic researchers through its Immunology Innovation Program (IIP), Argenx aims to translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines. Argenx is evaluating efgartigimod in multiple serious autoimmune diseases. Argenx is also advancing several earlier stage experimental medicines within its therapeutic franchises. The Director of Customer Management will support the International Region, currently focusing on Europe, the Middle East, and Australia in an above-country Medical Information (MI) delivery model. This role will ensure timely and accurate responses are provided to unsolicited medical and clinical inquiries from healthcare professionals, patients, clinical sites and other healthcare organizations. Roles and Responsibilities Responsible for prompt and accurate responses to medical information requests from internal and external customers through the MI Response Center, email, fax and websites for Europe, Middle East and Australia Responsible for ensuring the documentation of the inquiries and responses accurately and completely and are compliant with relevant Standard Operating Procedure (SOP)/ Work Instruction and applicable regulatory guidelines Ensures that adverse events and product quality complaints are processed in accordance with company SOPs Responsible for the creation, review and maintenance of MI documents by ensuring that responses are medically and scientifically accurate, timely, balanced, and meet customers’ needs Responsible for managing and training call center team including vendor and Argenx personnel Ensure the highest degree of quality and medical accuracy for all outputs developed Liaise with publications and clinical development groups to develop and maintain timely and relevant product expertise Perform critical analysis and synthesis of internal/external literature related to Argenx products and therapeutic areas of focus Supports internal teams by providing literature reviews and medical and scientific information related to Argenx therapeutic areas Exhibits broad knowledge of assigned therapeutics areas, product labelling and regulatory guidance Assists in maintenance of relevant knowledge repositories, including medical information responses and publications Appropriately liaise with Drug Safety and Quality regarding adverse events and product complaints, ensuring systematic capture and timely reporting Complete all work in accordance with regulatory requirements, industry standards, and Argenx procedures and policies Serves as medial affairs liaison to cross-functional groups for the incorporation of current medical/scientific information into department documents and processes. Develop/maintain metrics on key business processes to monitor Medical Information services through call centers Skills and Competencies Able to effectively network and partner with internal and external stakeholders and embrace cross-functional working Strong operational capabilities, eye for detail and commitment to advance and adhere to processes Able to identify inquirer’s question(s) and formulate and communicate an accurate response Able to search the published medical literature, evaluate published scientific information and create balanced and informative responses Understand and demonstrate the importance of providing superior customer service to all clients to support the business Excellent communication skills: verbal, written and when giving presentations Able to thrive as part of a team and when working independently Proven track record of delivering results that meet or exceed targeted objectives Detailed understanding of industry regulations and practices relating to medical information within Europe Ensures compliance and inspection/audit readiness Education, Experience and Qualifications PhD or PharmD or healthcare qualification (PharmD, PhD preferred) In addition to English, fluency in one or more European languages is preferred Experience in rare diseases is preferred 5+ years industry experience, working with medical information Experience managing medical information vendors Experience in inquiry management systems Experience in componentized content creation and content management system is preferred At Argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. Argenx is proud to be an equal opportunity employer. Before you submit your application, CV or any other personal details to us, please review our argenx Privacy Notice for Job Applicants to learn more about how Argenx B.V. and its affiliates (“Argenx”) will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at #J-18808-Ljbffr