Genmab
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Senior Clinical Drug Supply Manager
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Genmab . At Genmab, we are dedicated to building extraordinary futures together, by developing antibody products and groundbreaking therapies that change lives and the future of cancer treatment and serious diseases. We strive to create a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of patients, care partners, families and employees. Genmab is seeking an experienced Clinical Drug Supply Manager to join our Global Clinical Drug Supply Manufacturing team in Copenhagen or Princeton. The role requires candidates to be within commuting distance of our office locations and supports a hybrid work arrangement. The successful candidate will play a pivotal role in ensuring timely delivery of high-quality clinical trial supplies for both early and late-stage trials worldwide. As a Clinical Drug Supply Manager, you will manage the packaging and labeling of clinical supplies, review and approve GxP documentation, and collaborate closely with GMP QA and CMOs to ensure efficient packaging and labeling for patients with cancer and other serious diseases. You will also define appropriate drug supply activities at CMOs, contribute to SOPs and Work Instructions, perform training, and act as a subject matter expert while ensuring compliance with Genmab’s quality system. 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 Label, manage label translation with vendor and approval of label proofs/designs. Manage set‑up of distribution framework through service providers. Define appropriate drug supply activities at CMO necessary for providing drug supplies for clinical trials. Contribute to maintenance of SOPs and Work Instructions in the department. Perform training of other team members. Function as Subject Matter Expert within relevant areas. Responsible for being compliant with Genmab’s quality system. Qualifications
Bachelor’s degree in a relevant field (e.g., Pharmaceutical Sciences, Life Sciences, Healthcare, or Supply Chain Management). Minimum 3 years of experience in clinical drug supply management, including label text setup and ancillary handling. Demonstrated stakeholder management skills, both internally and externally. Experience working with vendors and CMOs for clinical trial supplies is an advantage. Solid knowledge of GDP and GMP. Knowledge of GCP is an advantage. Strong problem‑solving skills with the ability to excel in a fast‑paced, deadline‑driven environment. Excellent communication skills in English, both written and spoken. Highly organized with a structured, process‑oriented mindset supporting continuous improvement. Ability to prioritize effectively while maintaining a high level of quality and compliance. Strong interpersonal skills with the ability to work both independently and within 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 labeling clinical trial supplies, collaborating closely with the Global Clinical Drug Supply Execution team, the Global Clinical Drug Supply Systems team, and the Global Clinical Drug Supply Strategy team. Together, these four functions form the Global Clinical Drug Supply department, fostering a supportive, international, fast‑paced work environment centered on collaboration, excellence, and a can‑do attitude. 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. 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 U.S. based candidates, the proposed salary range is $122,000.00 – $183,000.00. 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. 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, our team has invented next‑generation antibody technology platforms and harnessed translational, quantitative, and data sciences to develop a proprietary pipeline of 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 antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with an international presence across North America, Europe, and Asia Pacific. For more information, 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).
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Senior Clinical Drug Supply Manager
role at
Genmab . At Genmab, we are dedicated to building extraordinary futures together, by developing antibody products and groundbreaking therapies that change lives and the future of cancer treatment and serious diseases. We strive to create a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of patients, care partners, families and employees. Genmab is seeking an experienced Clinical Drug Supply Manager to join our Global Clinical Drug Supply Manufacturing team in Copenhagen or Princeton. The role requires candidates to be within commuting distance of our office locations and supports a hybrid work arrangement. The successful candidate will play a pivotal role in ensuring timely delivery of high-quality clinical trial supplies for both early and late-stage trials worldwide. As a Clinical Drug Supply Manager, you will manage the packaging and labeling of clinical supplies, review and approve GxP documentation, and collaborate closely with GMP QA and CMOs to ensure efficient packaging and labeling for patients with cancer and other serious diseases. You will also define appropriate drug supply activities at CMOs, contribute to SOPs and Work Instructions, perform training, and act as a subject matter expert while ensuring compliance with Genmab’s quality system. 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 Label, manage label translation with vendor and approval of label proofs/designs. Manage set‑up of distribution framework through service providers. Define appropriate drug supply activities at CMO necessary for providing drug supplies for clinical trials. Contribute to maintenance of SOPs and Work Instructions in the department. Perform training of other team members. Function as Subject Matter Expert within relevant areas. Responsible for being compliant with Genmab’s quality system. Qualifications
Bachelor’s degree in a relevant field (e.g., Pharmaceutical Sciences, Life Sciences, Healthcare, or Supply Chain Management). Minimum 3 years of experience in clinical drug supply management, including label text setup and ancillary handling. Demonstrated stakeholder management skills, both internally and externally. Experience working with vendors and CMOs for clinical trial supplies is an advantage. Solid knowledge of GDP and GMP. Knowledge of GCP is an advantage. Strong problem‑solving skills with the ability to excel in a fast‑paced, deadline‑driven environment. Excellent communication skills in English, both written and spoken. Highly organized with a structured, process‑oriented mindset supporting continuous improvement. Ability to prioritize effectively while maintaining a high level of quality and compliance. Strong interpersonal skills with the ability to work both independently and within 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 labeling clinical trial supplies, collaborating closely with the Global Clinical Drug Supply Execution team, the Global Clinical Drug Supply Systems team, and the Global Clinical Drug Supply Strategy team. Together, these four functions form the Global Clinical Drug Supply department, fostering a supportive, international, fast‑paced work environment centered on collaboration, excellence, and a can‑do attitude. 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. 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 U.S. based candidates, the proposed salary range is $122,000.00 – $183,000.00. 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. 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, our team has invented next‑generation antibody technology platforms and harnessed translational, quantitative, and data sciences to develop a proprietary pipeline of 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 antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with an international presence across North America, Europe, and Asia Pacific. For more information, 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).
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