Senior Manager, Global Clinical Drug Supply
Jul 30, 2026 Copenhagen, Denmark
About us
- Size: 1,001-5,000 employees
- Industry: Biotechnology
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 (Senior) Clinical Drug Supply Manager to join Global Clinical Drug Supply (GCDS) Manufacturing in Copenhagen.
The successful candidate 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 Manufacturing function and cross-functionally to ensure scalability.
The (Senior) Clinical Drug Supply Manager will resolve complex operational challenges, lead strategic initiatives and mentor colleagues. 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.
The position reports to the Associate Director, Team Lead, Global Clinical Drug Supply Manufacturing based in Princeton.
Responsibilities
Responsibilities will be adjusted based on level of experience, and may include the following:
• Manage operational trial and project objectives related to packaging and labelling, providing proactive oversight to meet goals.
• Oversee inspection readiness and ensure compliance with relevant GMP, GDP and GCP regulations.
• 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 Manufacturing projects within the area of clinical drug supply management.
• Develop, maintain and implement SOPs for drug supply processes and manage cross-functional collaborations.
Qualifications
• Bachelor's degree in a relevant area (e.g., pharma, science, engineering, or supply chain management).
• Minimum 3 years of experience at manager level, and minimum 6+ years' experience for Senior Manager. Ideally demonstrated skills with global CMO vendor collaboration and oversight of clinical packaging and labelling activities.
• Demonstrated 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.
• Excellent communication skills in English, both oral and written.
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 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 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.
The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is:
DKK687.888,00---1.031.832,00
The final salary offer will depend on several factors, including your skills, qualifications, and experience.
In addition to base salary, this position is eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.
When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:
Further details on eligibility for compensation and benefits based on the role will be provided during the recruitment process.
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).
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 (Senior) Clinical Drug Supply Manager to join Global Clinical Drug Supply (GCDS) Manufacturing in Copenhagen.
The successful candidate 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 Manufacturing function and cross-functionally to ensure scalability.
The (Senior) Clinical Drug Supply Manager will resolve complex operational challenges, lead strategic initiatives and mentor colleagues. 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.
The position reports to the Associate Director, Team Lead, Global Clinical Drug Supply Manufacturing based in Princeton.
Responsibilities
Responsibilities will be adjusted based on level of experience, and may include the following:
• Manage operational trial and project objectives related to packaging and labelling, providing proactive oversight to meet goals.
• Oversee inspection readiness and ensure compliance with relevant GMP, GDP and GCP regulations.
• 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 Manufacturing projects within the area of clinical drug supply management.
• Develop, maintain and implement SOPs for drug supply processes and manage cross-functional collaborations.
Qualifications
• Bachelor's degree in a relevant area (e.g., pharma, science, engineering, or supply chain management).
• Minimum 3 years of experience at manager level, and minimum 6+ years' experience for Senior Manager. Ideally demonstrated skills with global CMO vendor collaboration and oversight of clinical packaging and labelling activities.
• Demonstrated 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.
• Excellent communication skills in English, both oral and written.
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 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 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.
The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is:
DKK687.888,00---1.031.832,00
The final salary offer will depend on several factors, including your skills, qualifications, and experience.
In addition to base salary, this position is eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.
When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:
- Pension
- Health insurance and wellness benefits
- Paid time off
- Employee support programs
Further details on eligibility for compensation and benefits based on the role will be provided during the recruitment process.
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).
Additional Information
- Posted: Jul 30, 2026