Manager, Global Clinical Drug Supply

Genmab

2d • Hybrid

About The Position

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 Clinical Drug Supply Manager to join our Global Clinical Drug Supply (GCDS) Execution team. This position is open to candidates based in Copenhagen or Princeton who reside within commuting distance of our office locations, supporting regular on-site collaboration as part of our hybrid way of working. Come and immerse yourself in an impressive pipeline and portfolio where you will be part of a team that plays a leading role in the planning and execution of clinical trial supplies and materials. You will apply your expertise to execute drug supply strategies, ensure adequate inventory levels, and collaborate closely with a wide range of stakeholders. Your work will directly support the timely delivery of high-quality clinical trial supplies and help bring innovative medicines to patients with cancer and other serious diseases. In addition, you will partner with key internal stakeholders, including multiple functions within CMC and members of the Clinical Trial Team (CTT), while providing guidance and coordination to external partners such as CROs and CMOs to ensure alignment and successful delivery. You demonstrate strong, professional written and verbal communication skills, enabling clear alignment and ensuring activities are executed as expected. You are an initiative-driven and proactive contributor who takes ownership and accountability for delivering high-quality clinical trial supplies on time from a planning and execution perspective. Operating in a dynamic environment where change is a natural part of the work, you are able to effectively prioritize tasks, balance urgency with importance, and adapt to evolving needs. This is a hybrid position reporting to the Global Clinical Drug Supply Execution Functional Lead, based in Princeton, NJ.

Requirements

• Minimum a bachelor’s degree or equivalent in relevant discipline
• Relevant work experience within the Pharmaceutical or biotechnology industry
• 3+ years’ of experience in clinical trial management or clinical drug supply activities is an advantage, including day-to-day forecasting, IRT systems, budgeting, and stakeholder management within CMC and Clinical development
• Solid knowledge and understanding of GCP, GMP, and GDP.
• Ability to work effectively in a fast-paced environment and with tight timelines.
• Proactive, goal oriented, and able to prioritize tasks effectively.
• Strong team player with a demonstrated ability to collaborate with a diverse range of internal and external stakeholders.
• Enjoys contributing to team spirit initiatives and actively embraces the collaborative and social culture within Drug Supply.
• Strong communication skills in English, both written and verbal.

Responsibilities

• Lead end-to-end trial execution activities from start-up to close out.
• Gather and maintain up-to-date project and trial information to support the execution of clinical drug supply strategies.
• Ensure timely planning, execution, and delivery of clinical trial supplies in alignment with study milestones and program strategy.
• Maintain all trial level inventory and ensuring no stock out situations.
• Actively participate in Clinical Trial Team (CTT) activities and meetings and other cross-functional forums to ensure aligned planning and execution.
• Early identification of risks and potential delays related to drug supply, inventory, or timelines, and develop mitigation and contingency plans.
• Participate in regulatory discussions in relation to IMP/AxMP
• Manage and maintain project/trial specific documentation (i.e. Trial Notification File (TNF), IMP manual, SIV slides, filing in eTMF etc.)
• Budget forecasting throughout the trial lifecycle
• Ensure GxP & regulatory guideline compliance during all drug supply planning tasks, activities, and deliverables
• Support inspection and audit preparation and execution.
• Participate in maintenance of SOPs.
• Participate in internal and cross-functional improvement projects
• Responsible for being compliant with Genmab’s quality system.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees