Senior Manager, Global Clinical Drug Supply (Comparator Sourcing)

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! The Role Genmab is searching for an experienced Senior Manager, Global Clinical Drug Supply, to be part of Global Clinical Drug Supply, Manufacturing in Copenhagen within commute distance from our office locations to work according to your hybrid work arrangement. With multiple late-stage trials progressing and increasing use of commercial medicinal products to support Genmab’s clinical trials, you will play a key role in ensuring high-quality supplies are sourced and delivered on time, supporting both early- and late-stage clinical trials. You will work closely with internal stakeholders and global vendors to keep supply activities on track, maintain accurate order information, and proactively identify and resolve issues that could impact timelines or availability. The scope of the individual contributor role will reflect your experience and will require strong prioritization. You will balance multiple parallel activities, keep critical details aligned across systems and teams, and ensure purchasing decisions are supported by accurate data and complete documentation. You bring structure and a collaborative mindset, feel comfortable navigating ambiguity, escalate when needed, and drive practical solutions across functions to help ensure supply reach patients reliably. The role reports to the Associate Director, Team Lead Global Clinical Drug Supply Manufacturing based in Copenhagen. Responsibilities Alignment across Global Clinical Drug Supply supporting supply for clinical trials. Monitor market dynamics (shortages, allocations, pricing shifts, supplier constraints) and provide actionable market intel to support supply continuity. Build and maintain strong relationships with global vendors and internal stakeholders to ensure supplies are available on time and in full. Review purchasing- and supply-related documentation/contracts and collaborate with Procurement/Legal/QA as needed to ensure appropriate terms and compliance. Contribute to budget planning/forecasting and cost management for sourced products; highlight risks and opportunities early. Drive maintenance and development of product sourcing related SOPs both internally and cross functionally including implementation of new regulations. Lead and participate in cross functional teams and support strategic cross functional collaboration. Execute sourcing activities in alignment with the current sourcing strategy and agreed sourcing approaches, ensuring consistent ways of working and audit-ready documentation. Set standards for operational work and compliance and support overall strategic direction and development in department. Responsible for being compliant with Genmab´s quality system. Requirements Minimum a bachelor’s degree or equivalent. Minimum 6+ years’ experience in a regulated environment (Biotech/Pharma/Clinical Supply/Procurement/Supply Chain or similar). Ideally involving global vendors and operational purchasing. Experience working with CMO for clinical supplies including vendor management. Extensive experience in driving and contributing to large cross functional projects with an innovative and entrepreneurial attitude. Comfortable working with a mix of administrative and coordination tasks, while keeping a strong focus on accuracy, timelines, and stakeholders. Extensive knowledge and understanding of GMP, GDP, and GCP. High proficiency in spend analysis, market intelligence and supplier performance management. Proven experience working in global, virtual and cross-functional teams. Thrive in a rapidly changing environment with tight timelines, juggling multiple tasks while keeping strong attention to detail. Curious, self-driven, and confident asking questions and speaking up when something doesn’t add up. Collaborative team player who works well with diverse internal stakeholders and global partners, motivated by patient impact. Strong communication skills in English - both oral and written. The Team You will join a highly competent team focused on packaging and labelling of clinical supplies, collaborating closely with the Global Clinical Drug Supply Execution team. Together with the Global Clinical Drug Supply Systems team and Global Clinical Drug Supply Strategy team, these four functions form the Global Clinical Drug Supply department. We have an international and informal working environment with a high pace while having fun and focusing on one team spirit both within and outside the team and department. Application If this opportunity excites you, we encourage you to upload your CV and cover letter outlining your motivation for the position. Applications are reviewed on a rolling basis, and interviews will be scheduled accordingly. Please note, fully remote applicants will not be considered; candidates must be within commuting distance of Copenhagen. The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is: DKK0,00---0,00 The final salary offer will depend on several factors, including your skills, qualifications, and experience. In addition to base salary, this position is eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives. When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to: Pension Health insurance and wellness benefits Paid time off Employee support programs Further details on eligibility for compensation and benefits based on the role will be provided during the recruitment process. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X . Genmab is committed to protecting your personal data and privacy. 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