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 a Clinical Drug Supply Manager to join our Global Clinical Drug Supply (GCDS) Operations Team in Princeton or Copenhagen within commute distance from our office locations to work according to our hybrid work arrangement.

Responsibilities/tasks:

Act as Clinical Drug Supply Manager, of the following tasks:

• Obtain Project/Trial specific information to initiate drug supply strategic planning and execution, and maintain information on changing clinical development plan

• Identify risks for delays for projects/programs and trials and possible mitigations (contingency plans and new/additional scenarios) that may impact clinical drug supply)
• Create and maintain program/project and trial IMP/AMP forecast and demand plans throughout the trial lifecycle
• Maintain all project/program trial level inventory and ensuring no stock out situations
• Create and maintain program/project and trial budget forecast throughout the trial lifecycle
• Lead and participate in cross functional teams (CDTs, CSTs, CTTs, CMC) and support strategic cross functional collaboration (i.e., project/program and trials
• Lead/Participate in Clinical Project Supply Team discussion
• Participate in regulatory discussions in relation to IMP/AMP
• Manage project/trial specific planning documentation (i.e., drug supply plan, milestone tracking, IMP manual, etc.
• Ensure GxP compliance & regulatory guideline compliance during all drug supply planning tasks, activities, and deliverables

Global Clinical Drug Supply:

• Support development and maintenance of SOPs for the Global Clinical Drug Supply Operation area including implementation of new regulations in the department
• Provide SME knowledge support
• Coach and mentor colleagues during onboarding and maintenance of training
• Responsible for oversight and resolution of deviations, CAPAs and change controls in connection to Clinical Drug Supply Operation
• Drive Inspection and Audit preparation and execution
• Responsible to be compliant with Genmab’s quality system

Requirements

• Minimum a Bachelors with 3-5 years experience.  Master’s degree with +2 years experiences, or PhD’s degree with +1 year of experience, or equivalent of experience.
• Experience in handling supply chain, manufacturing, ERP, clinical supply chain, operations, logistics, preferably in the pharmaceutical or biopharmaceutical industry.
• Broad and Diverse experience in working with trial management for global clinical drug supply and supply functions
• Knowledge and understanding of GMP, GDP, and GCP. Supply Chain systems and processes.
• Strong desire to exploit emerging technologies for better business outcomes.
• Proven experience working in teams.
• Ability to work successfully under pressure in a fast-paced environment and with tight timelines.
• Ability to be proactive, enthusiastic, and goal orientated.
• A team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders to support the execution of tasks.
• Strong communication skills in English - both oral and written.

The Team

You will be part of a highly competent team focused on planning and maintenance of supplies for clinical trials, working closely with the Global Clinical Drug Supply Operations & System team and our cross-functional stakeholders.

Together with Global Clinical Drug Supply Operations & Systems team the three teams make up the Global Clinical Drug Supply department.

We have an international and informal working environment with a high pace while having fun and focus on one team spirit both within and outside the team and department.

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 bonuses. 

Regular full-time U.S. employees are eligible to enroll in Genmab benefits. Our benefits package is crafted to help employees feel supported and cared for in all aspects of life — physical, financial, social, and emotional. 
 

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!

Locations

Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our 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 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.