Genmab
Overview
Join to apply for the
IRT Manager
role at
Genmab Genmab is seeking an experienced
IRT/System Manager
to join our
Global Clinical Drug Supply, Technical Operations
team. The position is in
Copenhagen
and requires onsite presence 3 days/week according to company policy. The Role & Department
With a strong pipeline and numerous ongoing clinical trials, you will play a key role in
IRT Management —ensuring timely and high-quality clinical trial supplies for both early- and late-stage studies that support patients battling cancer and other serious diseases. We are looking for proactive, solution-oriented professionals who thrive in dynamic environments, can balance priorities, and adapt quickly to change. Our workplace is international, fast-paced, and collaborative—driven by a strong “one team” spirit both within and across departments. Responsibilities
IRT Portfolio & Project Management
Oversee the full lifecycle of trial-specific IRT systems (setup, maintenance, decommissioning). Coordinate IRT implementation, protocol-driven requirements, UAT planning/execution, integrations, documentation, and training. Ensure adherence to IRT system standards and proactively manage risks. Oversee multiple projects, ensuring schedules and deliverables are met in collaboration with cross-functional stakeholders. Communicate project status effectively and participate in operational planning sessions. IRT Vendor Management
Support KPIs, metrics, and trend analysis to anticipate and mitigate risks. Provide oversight of vendor activities, ensuring quality and compliance. Collaborate with vendor project managers for assigned trials and support in audits and inspection readiness. Facilitate problem resolution, root cause analysis, and corrective actions. Continuous Improvement
Provide inputs for areas and opportunities to improve processes. Support cross-functional training and initiatives. May provide support for the creation / maintenance of documentation, such as, but not limited to SOPs, work instructions, and job aids. Requirements
Bachelor’s degree in a scientific or technical field; advanced degree/certification preferred. 2+ years’ experience in supply chain or related areas within pharma, biotech, or medical devices. Strong knowledge of regulatory standards (e.g., GMP, GCP, ICH). Hands-on experience with IRT systems preferred. Proven ability to manage large projects with multiple stakeholders. Experience working in cross-functional, multicultural teams. For US based candidates, the proposed salary band for this position is as follows: $97,120.00 – $145,680.00 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! 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. Seniority level
Mid-Senior level Employment type
Full-time Job function
Management and Manufacturing
#J-18808-Ljbffr
Join to apply for the
IRT Manager
role at
Genmab Genmab is seeking an experienced
IRT/System Manager
to join our
Global Clinical Drug Supply, Technical Operations
team. The position is in
Copenhagen
and requires onsite presence 3 days/week according to company policy. The Role & Department
With a strong pipeline and numerous ongoing clinical trials, you will play a key role in
IRT Management —ensuring timely and high-quality clinical trial supplies for both early- and late-stage studies that support patients battling cancer and other serious diseases. We are looking for proactive, solution-oriented professionals who thrive in dynamic environments, can balance priorities, and adapt quickly to change. Our workplace is international, fast-paced, and collaborative—driven by a strong “one team” spirit both within and across departments. Responsibilities
IRT Portfolio & Project Management
Oversee the full lifecycle of trial-specific IRT systems (setup, maintenance, decommissioning). Coordinate IRT implementation, protocol-driven requirements, UAT planning/execution, integrations, documentation, and training. Ensure adherence to IRT system standards and proactively manage risks. Oversee multiple projects, ensuring schedules and deliverables are met in collaboration with cross-functional stakeholders. Communicate project status effectively and participate in operational planning sessions. IRT Vendor Management
Support KPIs, metrics, and trend analysis to anticipate and mitigate risks. Provide oversight of vendor activities, ensuring quality and compliance. Collaborate with vendor project managers for assigned trials and support in audits and inspection readiness. Facilitate problem resolution, root cause analysis, and corrective actions. Continuous Improvement
Provide inputs for areas and opportunities to improve processes. Support cross-functional training and initiatives. May provide support for the creation / maintenance of documentation, such as, but not limited to SOPs, work instructions, and job aids. Requirements
Bachelor’s degree in a scientific or technical field; advanced degree/certification preferred. 2+ years’ experience in supply chain or related areas within pharma, biotech, or medical devices. Strong knowledge of regulatory standards (e.g., GMP, GCP, ICH). Hands-on experience with IRT systems preferred. Proven ability to manage large projects with multiple stakeholders. Experience working in cross-functional, multicultural teams. For US based candidates, the proposed salary band for this position is as follows: $97,120.00 – $145,680.00 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! 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. Seniority level
Mid-Senior level Employment type
Full-time Job function
Management and Manufacturing
#J-18808-Ljbffr