(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, or Princeton 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 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.

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 3 years of experience at manager level, and 6+ years' experience in a regulated environment (Biotech/Pharma/Clinical Supply/Procurement/Supply Chain or similar) for Senior Manager. 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 or Princeton or willing to relocate.

For US based candidates, the proposed salary band for this position is as follows:

$126,480.00---$189,720.00

The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.


When you join Genmab, you're joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:

• 401(k) Plan: 100% match on the first 6% of contributions
• Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
• Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
• Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
• Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
• Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

About You

• You are genuinely passionate about our purpose
• You bring precision and excellence to all that you do
• You believe in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds
• You take pride in enabling the best work of others on the team
• You can 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 maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our 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 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. 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.