Global Medical Indication Lead

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.

Global Medical Indication Lead (Rheumatology)

• Provide continuous strategic medical insight and planning for the indication during all the stages of development
• Own the Clinical development plan and participate in long‑range strategic planning as data emerges in the indication
• Line‑manage the Global Clinical Trial Physicians working on the indication. Provide coaching and set example for the team ensuring high‑quality medical support for the study teams
• Real‑time oversight of the medical aspects of studies in the indication, including the relevant communication to management as well as the different study teams
• Safeguard harmonization across the studies so that communications to external stakeholders (e.g., questions of IRBs, RAs) are consistent and company efficiency is maintained in close collaboration with peers as well as management of the different functional groups
• Lead indication medical advisory boards as appropriate
• Help build and maintain a “best in class” group of development medical doctors
• Ensure compliance of all studies in the indication

• Medical Doctor with relevant specialty education preferred (e.g., neurology, hematology, dermatology, immunology, rheumatology, internal medicine, pediatric)
• At least 3–5 years in the pharma/biotech industry, having acquired an in-depth understanding of end‑to‑end (phase I to registration) drug development
• Excellent English, both written and spoken, is a must, as well as ability to travel
• Proven leadership, motivational and interpersonal skills in a global and intercultural environment, including leading through influence
• Pro‑active problem‑solver with negotiation skills
• Must provide clear vision, direction, and purpose to the different study teams
• Demonstrated expertise in clinical trial design, conduct and interpretation of clinical data
• Strong communication skills to ensure that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties
• Additional skills in gathering decision information, negotiation and communicating decisions and action
• Executes responsibilities with knowledge, accuracy, persistence, resilience and creativity, being an accomplished team player whilst maintaining medical integrity

This job is eligible to participate in our short‑term and long‑term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines.

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.

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