Senior Manager, Global Clinical Drug Supply

At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose. The Role & Department Genmab is seeking an experienced Senior Clinical Drug Supply Manager to join our Global Clinical Drug Supply Operations team. As Senior Clinical Drug Supply Manager you will play a pivotal role in ensuring the timely delivery of high-quality clinical trial supplies for both early and late-stage trials. In addition, this position offers significant influence over the refinement of Genmab’s processes, both within the GCDS Operations team and cross-functionally to ensure scalability. It is expected that you will take lead of strategic initiatives, mentor colleagues, and resolve complex operational challenges. A key focus of this role will be supporting team members through troubleshooting, problem-solving, and developing mitigation plans for complex issues related to packaging and labelling activities. This role requires balancing urgency and importance in a dynamic environment while serving as a positive role model for the team, by bringing a strong can-do attitude to drive solutions and inspire others. You will join a highly competent global team focused on packaging and labeling clinical trial supplies, collaborating closely with the Global Clinical Drug Supply Planning team. Together with the Global Clinical Drug Supply Systems team, these groups form the Global Clinical Drug Supply department. We foster a supportive, international, and fast-paced work environment centered on collaboration, excellence, and a can-do attitude to achieve results. You will be reporting to Director, Global Clinical Drug Supply in Copenhagen, Denmark. Main Responsibilities Include Engage with internal and external stakeholders to ensure alignment and successful collaboration. Supervise and monitor vendor performance, ensuring delivery aligns with timelines and SOW. Provide direct support to team members in troubleshooting and problem resolution, ensuring effective development of mitigation plans for operational challenges. Mentor and coach team members, fostering a collaborative and high-performing environment. Lead complex GCDS Operations projects within the area of clinical drug supply management. Oversee inspection readiness and ensure compliance with relevant regulations. Manage operational trial and project objectives, providing proactive oversight to meet goals. Develop, maintain and implement SOPs for drug supply processes and manage cross-functional collaborations. Requirements You hold a Bachelor’s degree in a relevant area (e.g., pharma, science, engineering, or supply chain management). Come with + 7 years of demonstrated ability managing clinical drug supply, including label text setup, ancillary handling, and cold chain management. Proven experience working with CMOs for clinical trial supplies, including vendor management. Ability to lead cross-functional projects with an innovative and entrepreneurial mindset. Collaborative, proactive, and goal-oriented team player who inspires colleagues while fostering strong relationships. Strong problem-solving skills and ability to thrive in a fast-paced, deadline-driven environment. Extensive knowledge of GMP, GDP, and GCP regulations. Effective communication skills in English, both oral and written. The position will be based in our Copenhagen or Princeton site, which require onsite presence 60% of the time as per our hybrid policy. About You You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving You are a generous collaborator who can work in teams with diverse backgrounds You are determined to do and be your best and take pride in enabling the best work of others on the team You are not afraid to grapple with the unknown and be innovative You have experience working in a fast-growing, dynamic company (or a strong desire to) You work hard and are not afraid to have a little fun while you do so Locations Genmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories. Whether you’re in one of our collaboratively designed office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies. 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 locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan.  Our commitment to diversity, equity, and inclusion We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information. Learn more about our commitments on our website .  Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com) . Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.