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!
Job TitleClinical Trial Operations Intern
Why GenmabAt Genmab, interns don't just learn about the work - they help move it forward. Our internship program provides meaningful, hands-on experience through real projects that directly support our teams, business priorities, and mission to transform the lives of people with cancer and other serious diseases.
From day one, interns are welcomed as part of the team and given opportunities to contribute, collaborate, and make an impact. Along the way, you'll learn from talented colleagues and senior leaders, build new skills, expand your professional network, and gain exposure to the innovative work happening across Genmab.
We're always looking for smart, curious, purpose-led people who are ready to bring fresh perspectives and bold ideas. Explore our website to learn more about Genmab and how you could play a role in our bold, extra[not]ordinary® future.
Job OverviewAs a Clinical Trial Operations Intern, you will gain hands-on exposure to clinical trial planning, operations, and delivery. You will contribute to projects that strengthen Genmab's clinical trial execution capabilities through process improvement, data-driven insights, and operational excellence. Working cross-functionally with experts in Clinical Operations, Vendor Oversight and Standards, Clinical Data, Integration & Reporting, and Trial Planning, you'll apply both scientific and technical skills to enhance clinical trial efficiency and execution; documenting clinical operation practices that are consistent, scalable, and inspection ready.
This role is ideal for individuals pursuing advanced studies in life sciences, biomedical engineering, or related fields, with a strong interest in clinical research, regulatory systems, and project management.
What you'll doInterns will contribute to one or more of the following initiatives:
- Process optimization and quality documentation
Contribute to designing compliant processes and assist in ensuring high-quality documentation aligned with regulatory standards. - Business and clinical trial operations
Support enhancements and/or building new operational tools leveraging AI, PowerBI or other software, including requirements gathering, testing, and process documentation.
- Inspection readiness and trial documentation
Develop a practical readiness toolkit by reviewing trial documentation, identifying common gaps, and creating checklists or dashboards that support consistent, inspection-ready execution.
- Trial performance metrics and insights
Analyze operational data to identify trends, bottlenecks, and improvement opportunities, and develop clear visualizations or summaries for study teams and leadership.
- Knowledge management and digital enablement
Organize clinical operations guidance and lessons learned into accessible resources and explore responsible uses of automation or AI to improve information retrieval and team collaboration.
Required qualifications, capabilities and skills- Currently pursuing a Bachelor's degree (Junior or Senior standing) or Master's degree in Life Sciences, Biomedical Engineering, Drug Discovery and Development, or a related discipline
- Strong analytical and organizational skills with proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, SharePoint) and comfort with AI and/or PowerBI to solve complex problems.
- Demonstrated ability to manage data, documentation, or process improvement projects.
- Excellent communication, teamwork, and problem-solving skills.
Preferred qualifications, capabilities and skills- Experience using or classwork in Lean, Six Sigma and/or Project Management practices.
- Knowledge or experience in GxP practices or ICH guidelines.
- Experience with Planisware, Veeva Vault, or other trial management systems.
- Background in clinical operations, drug development, or medical technology research.
General Intern Information - Date/Location/ScheduleInternships will take place over 10 weeks from June - August 2027. This role will be based in Princeton, NJ and operate on a required hybrid schedule - 3 days in the office and 2 days remote per week. This role is not eligible for work visa sponsorship at the time of the application or in the future.
What's next?Help us learn about you by submitting a complete and thoughtful application, which includes your resume. Your application and resume are a way for us to initially get to know you, so it's important to complete all relevant questions to ensure we have as much information about you as possible.
Every application matters to us, and we'll carefully review each submission as quickly as possible to see if your qualifications align with the role. While we're unable to provide individual updates, rest assured that we're working diligently to move through the process efficiently.
If you move forward in the process, you'll receive an email invitation to connect with us and dive deeper into this exciting opportunity. The final stage will bring selected candidates meeting directly with our hiring teams, where you'll have the chance to showcase your potential. We are committed to keeping you informed and will share decisions with all candidates as soon as we are able. We can't wait to see where this journey takes you!
About GenmabGenmab 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
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