At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
Clinical Trial Manager – Join Genmab’s Global Team
At Genmab, we’re looking for a Clinical Trial Manager to join our dynamic Trial Strategy and Delivery team of over 75 passionate professionals in Denmark, the US, the Netherlands, and Japan. In this role, you’ll handle critical trial activities such as vendor oversight, site selection, and operational setup (e.g., DM, IRT, and eRT) while being part of a team that thrives on collaboration, innovation, and a “knock-your-socks-off” spirit. From Day One, our comprehensive onboarding program will ensure you’re ready to succeed with the support of mentors, colleagues, and collaborators.
Responsibilities
As a Clinical Trial Manager, you’ll take charge of a variety of key responsibilities, including:
Developing operational plans, charters, and trial manuals.
Reviewing trial protocols, amendments, and other critical trial documents.
Leading the creation of the Trial Oversight Plan and Global Master ICF, including amendments.
Coordinating site selection with the Start-Up team, reviewing regulatory documents, and approving site activations.
Supervising vendor management, including vendor results, and ensuring alignment on trial activities.
Supporting trial execution by leading protocol deviations, supervising KPIs/KQIs, resolving site issues, and participating in Risk-Based Quality Management (RBQM) activities.
Collaborating with cross-functional teams to address escalations and ensure timely issue resolution.
Participating in inspection readiness, audits, and site monitoring oversight activities as needed.
Requirements
Experience: A Bachelor’s or master’s in medical, biological, or pharmaceutical sciences (or equivalent). With 3-5+ years of experience in clinical trial management from a pharmaceutical company and/or CRO, ideally within oncology or first-in-human trials.
Expertise: Strong knowledge of trial execution, GCP, and clinical drug development, with experience operating in a global setting.
Skills: Exceptional communication skills (written and verbal), risk management abilities, and stakeholder management.
Soft Skills: A proactive problem solver who identifies risks and develops effective mitigations. A collaborative leader with a quality mindset, adaptability in fast-paced environments, and the ability to inspire trust.
Ready to Grow?
This role can be elevated to a Senior level based on your experience. Join us at Genmab and be part of a team dedicated to making a lasting impact on oncology research!
About You
Locations
Genmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories. Whether you’re in one of our collaboratively designed 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 guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies. 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 locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan.
Our commitment to diversity, equity, and inclusion
We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information. Learn more about our commitments on our website.
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.
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