Clinical Drug Supply Manager

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
Genmab is seeking an experienced Clinical Drug Supply Manager to join our Global Clinical Drug Supply Operations in Copenhagen or Princeton. The position requires candidates to be within commuting distance of one of our office locations to accommodate our hybrid work arrangement. In this role, you will be instrumental in ensuring the timely delivery of high-quality clinical trial supplies for both early- and late-stage clinical trials.

As a Clinical Drug Supply Manager, you will manage the packaging and labeling of clinical supplies, ensuring their efficient delivery for Genmab’s global clinical trials. A key responsibility will be reviewing and approving GxP documentation to ensure adherence to the highest quality standards during production at our CMOs. You will collaborate closely with GMP QA and our CMOs to ensure timely packaging and labeling for clinical trials focused on treating cancer and other serious diseases.

The ideal candidate will have a solid understanding of cGMP and a strong commitment to delivering high-quality work, demonstrating a proactive approach and a willingness to go above and beyond to achieve the best possible outcomes for patients.

The position reports to the Director of Global Clinical Drug Supply Operations based in Copenhagen.

Responsibilities

• Manage and coordinate drug supply and provide IMP for clinical trials.
• Manage and coordinate ancillaries, pre-medication, and comparators for clinical trials.
• Set-up English Master Labels, manage label translations with our vendors and approve label proofs/designs.
• Manage the setup of the distribution framework through service providers.
• Define the necessary drug supply activities at CMOs to support the provision of drug supplies for clinical trials.
• Contribute to the maintenance and updates of SOPs and Work Instructions within the department.
• Provide training to other team members.
• Function as Subject Matter Expert within relevant areas.
• Responsible for being compliant with Genmab’s quality system.

Requirements

• Bachelor’s degree in a relevant field (e.g., Pharmaceutical Sciences, Life Sciences, Healthcare, or Supply Chain Management).
• Minimum of 5 years of experience in clinical drug supply management, including label text setup, ancillary handling.
• Demonstrated stakeholder management skills, both internally and externally.
• Experience working with vendors and CMOs for clinical trial supplies will be an advantage.
• Solid knowledge of GDP and GMP. Knowledge of GCP will be an advantage.
• Strong problem-solving abilities with the capacity to thrive in a fast-paced, deadline-driven environment.
• Excellent communication skills in English, both written and spoken.
• Highly organized with a structured, process-oriented mindset focused on continuous improvement.
• Ability to prioritize tasks effectively while maintaining a high standard of quality and compliance.
• Strong interpersonal skills, capable of working both independently and as part of global teams.
• Results-driven and goal-oriented, committed to contributing to Genmab’s success.

The Team
You will join a highly competent team focused on packaging and labelling 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.

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.

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.

Location: Copenhagen - Carl Jacobsens Vej 30

Additional location:

• Princeton