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!
The Role
Genmab is looking for a Director, EU/ROW Regulatory Lead to be a part of our Global Regulatory Affairs organization.
In this role, the candidate will represent RA in the Clinical Trial Teams and work closely with the CRO and internal stakeholders to ensure regulatory oversight and progress of the clinical trial submissions in EU/ROW. The candidate may also be allocated as EU/ROW Regulatory Strategy Lead to one or multiple compounds in early or late development and provide regulatory expertise and guidance on EU/ROW procedural matters and documentation requirements to the Global Regulatory Team and Compound Development Team to ensure an optimal EU/ROW regulatory strategy for the compound.
The position is based in Utrecht/NL and will report to the EU/ROW Regulatory Strategy Team Lead.
Responsibilities
The responsibilities of the role will include, but is not limited to:
- Represent RA in the Clinical Trial Teams and ensure oversight and progress of multiple, often highly complex, clinical trial submission activities.
- Represent EU/ROW in the Global Regulatory Team(s).
- Act as EU/ROW Regulatory Lead for the assigned project(s) and be responsible for the development and execution of the EU/ROW regulatory strategy.
- Lead the preparation of strategic regulatory documents, e.g. Briefing Packages, ODDs, PIPs, etc.
- Plan, prepare and lead EMA or national Scientific Advice procedures, as relevant.
- Evaluate regulatory risks and recommend mitigation strategies to the cross-functional teams and management.
- Monitor and assess regulatory guidelines and regulations and current regulatory environment/landscape and their impact on the development of Genmab products.
- Maintain an updated knowledge of regulatory topics and regulations and participate in maintaining and preparing regulatory processes and ways of working.
Requirements
- A minimum of Bachelor’s degree or equivalent in scientific discipline or health-related field. Master’s degree preferred.
- Minimum of 8 years of experience in Regulatory Affairs, preferably in development phase up to and including submission of global marketing authorization applications.
- Experience in proactively planning and executing highly complex clinical submission strategies.
- Prior experience leading health authority meetings with the EMA or other health authorities.
- A good understanding of drug development and EU regulatory procedures.
- Experience within oncology and/or I&I will be a plus.
- Experience with PIPs will be a plus.
- Experience with development and regulatory requirements in ROW markets will be a plus.
- Strong project management skills.
Moreover, you meet the following personal requirements:
- Strong organizational, communication, and time management skills needed to lead multiple ongoing projects simultaneously.
- Must have attention to detail and be able to solve problems with minimal supervision.
- Be able to work independently with an ability to drive projects to successful outcomes.
- Robust cross-functional teamwork skills and enjoy working in a global environment.
- Skills in building and maintaining internal and external collaborative relationships to achieve shared goals.
- Highly motivated and dedicated individual who enjoys being challenged.
- Able to prioritize your work in a fast paced and changing environment.
- Goal-oriented and committed to contributing to the overall success of Genmab.
Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly motivated team members across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.
The proposed gross annual base salary range for this position, in the primary location, based on a full time schedule is:
EUR96.000,00-144.000,00

The final salary offer will depend on several factors, including your skills, qualifications, and experience.
In addition to base salary, this position is eligible to additional forms of compensation, such as discretionary bonuses and long-term incentives.
When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:
- Pension
- Health insurance and wellness benefits
- Paid time off
- Employee support programs
Further details on compensation and benefits will be provided during the recruitment process.
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 contract.
