Senior Clinical Drug Supply Manager

At Genmab we are dedicated to building extranotordinary 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 Clinical Drug Supply Manager to join our Global Clinical Drug Supply Manufacturing in Copenhagen or Princeton. The role requires candidates to be within commuting distance of our office locations to work according to our hybrid work arrangement. 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.

As a Clinical Drug Supply Manager you will play a pivotal role in ensuring efficient delivery of high-quality clinical trial supplies for both early and late-stage Genmab clinical trials worldwide. Your responsibilities will include managing the packaging and labelling of clinical supplies. A key aspect of this role is review and approval of GxP documentation ensuring the highest quality standards is adhered to during production at our CMOs. You will collaborate closely with GMP QA and our CMOs ensuring timely packaging and labelling for our clinical trials for patients with cancer and other serious diseases.
The ideal candidate possesses an understanding of cGMP and a strong commitment to delivering high-quality work demonstrating a proactive approach and willingness to go the extra mile to ensure the best outcome for patients.

This position is hybrid and requires you to be in the office 60% of the position reports to the Associate Director Team Lead Global Clinical Drug Supply Manufacturing 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 Label manage label translation with our 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 Genmabs quality system.

Qualifications
Bachelors 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 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 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 that supports 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 Genmabs 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 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 or Princeton or willing to relocate.

For US based candidates the proposed salary band for this position is as follows:

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 youre 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!

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 youre 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 Genmabs 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 and follow us on LinkedIn and X.

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Please note that if you are applying for a position in the Netherlands Genmabs 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.