Senior Manager, Global 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!

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.

• 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.

• Pension
• Health insurance and wellness benefits
• Paid time off
• Employee support programs