Senior IRT Manager, Clinical Drug Supply

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! Genmab is seeking an experienced Senior IRT Manager to join our Global Clinical Drug Supply Systems team. In this role, you will provide senior-level leadership for the design, implementation, and lifecycle management of Interactive Response Technology (IRT) solutions supporting Genmab’s global clinical development portfolio. As a Senior IRT Manager, Global Clinical Drug Supply, you will lead complex and strategically important clinical trial IRT implementations while serving as a subject matter expert across IRT platforms, processes, and standards. You will partner closely with Clinical Operations, Data Management, Clinical Supply, Quality, and external IRT vendors to ensure systems are delivered with the appropriate quality, compliance, scalability, and operational effectiveness throughout the clinical trial lifecycle. Beyond individual trial delivery, you will contribute to the continued evolution of Genmab’s IRT capabilities by helping shape standards and best practices, evaluating platform changes and emerging capabilities, supporting vendor governance, and leading cross-trial improvement initiatives. The ideal candidate brings strong IRT and clinical development experience, a solid understanding of GxP and computerized system requirements, and the ability to navigate complex cross-functional and vendor relationships. We are looking for someone who combines technical and operational expertise with proactive problem solving, clear communication, and a strong commitment to quality and ultimately to supporting the patients who participate in Genmab clinical trials. Work arrangement: This role offers flexibility to work away from the office for 20%–40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager. Responsibilities: IRT Portfolio and Complex Trial Leadership Independently lead complex, high-priority, or strategically significant trial-specific IRT systems across the full system lifecycle. Provide IRT leadership across programs or related groups of clinical trials where alignment of design, standards, vendors, or operational approaches is required. Anticipate portfolio-level risks, dependencies, and opportunities and proactively recommend mitigation or improvement strategies. Serve as a senior escalation and consultation resource for IRT Managers on complex design, operational, quality, and vendor issues. Lead resolution of significant IRT issues requiring cross-functional coordination and independent judgment. IRT Platform and Standards Leadership Serve as subject matter expert for one or more IRT platforms, processes, standards, or technical capability areas. Lead or significantly contribute to development, refinement, and implementation of IRT standards, best practices, procedures, and training. Evaluate vendor platform changes and new capabilities and assess operational, compliance, and trial impacts. Lead assigned platf…

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