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 searching for an experienced Senior Clinical Drug Supply Manager to be part of Global Clinical Drug Supply (GCDS) Planning in Copenhagen or Princeton within commute distance from our office locations to work according to your hybrid work arrangement.

Come and immerse yourself in an impressive pipeline and portfolio where you will have the opportunity to be part of the team that is in the leading role in the planning of clinical trial supplies and materials. The individual will have the ability to exercise their skills and knowledge on forecasting scenario planning and stakeholder management. Leading and supporting this type of work will allow the individual to be at the forefront of bringing medicines to cancer patients and other serious disease.

Senior Clinical Drug Supply Manager team will work in partnership with several internal and external stakeholders including GCDS Operations GCDS Systems Development Operations Portfolio & Project Management and CMC. The role will also help guide CROs CMOs clinical site personnel and medical affair steam.

You are skilled in professional and clear written and oral communication to ensure activities are carried out as per expectation. You must be an initiative driven and proactive player with responsibility to deliver high quality trial supplies on time from a planning perspective. Changes are a natural part of our work so you are able prioritize your tasks and balance importance with urgency.

The position is hybrid and reports to the Global Clinical Drug Supply Planning Leader based in Princeton NJ.

Responsibilities
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 plans trial IMP/AxMP forecast and demand plans and budgets throughout the trial lifecycle
Maintain all project/program trial level inventory and ensuring no stock out situations.
Lead and participate in cross functional teams and support strategic cross functional collaboration (i.e. project/program and trials)
Lead Clinical Project Supply Team discussions.
Participate in regulatory discussions in relation to IMP/AxMP
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
Support inspection and audit preparation and execution.
Participate in maintenance of SOPs.
Responsible to be compliant with Genmabs quality system.

Requirements
Minimum a bachelors degree or equivalent.
Advantage with 6 years experience in handling clinical drug supply including forecasting demand planning budgeting and project planning
Experience in working with trial management for clinical trial supplies.
Knowledge and understanding of GMP GDP and GCP.
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:

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.