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 TitleStandards and Systems 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 OverviewThe Standards and Systems Intern will support Genmab's data standards, clinical systems, and standards governance activities by gaining hands-on experience in key components of clinical data management during a 10-week summer internship.
This role provides practical exposure to the foundational elements that ensure consistency, quality, and compliance in clinical data collection across Genmab trials. Working closely with the Standards & Systems team, the intern will develop an understanding of Genmab's core standards requirements, including Case Report Form (CRF) design, edit check testing and validation, processing standards change request and Service Now Request related to EDC system user access, all through direct assignments and mentorship. The intern will also contribute to continuous process improvement initiatives by offering suggestions and completing assigned tasks that enhance departmental efficiency and quality.
In addition to supporting the Standards & Systems team, the intern will collaborate with cross-functional teams, contributing to process improvements, development activities, and other projects that have a tangible impact on Genmab's drug development efforts.
What you'll do- Contribute to meetings within the standards and systems group
- Assist in the intake, review, and documentation of Standards Change Requests
- Participate in internal alignment discussions and cross-functional meetings related to implementation of standards
- Participate in validation activities for the build of standard Case Report Forms (CRFs) and edit checks
- Assist in updating and maintaining the Genmab Standard CRF Template and Allowable Modification and Usage (AMU) Guide
- Assist with filing standards and system documentation within eTMF, ensuring accuracy and inspection readiness
- Help process ServiceNow requests for EDC user access and monitor compliance with access-control procedures
- Maintain and update the Standards & Systems SharePoint site, ensuring that content is current, organized, and accessible
- Attend standards and systems departmental meetings and/or study team meetings as required
- Contribute to drafting, updating, and improving departmental process documents, workflows, and best-practice guides
Required qualifications, capabilities and skills- Enrollment in a Bachelor or Master's program in Health Sciences, Data Science, or a related field.
- Basic understanding of clinical trial regulatory environment.
- Strong analytical and problem-solving abilities.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a collaborative team.
- High attention to detail and commitment to quality work.
- Genuine interest in clinical research and drug development.
Preferred qualifications, capabilities and skills- Demonstrates initiative, a proactive attitude, and eagerness to learn in a fast-paced environment.
- Effectively communicates and collaborates with team members, mentors, and stakeholders.
- Applies academic expertise in open-source programming languages and adapts quickly to new tools and methodologies.
- Maintains attention to detail and quality in all deliverables while managing multiple tasks.
- Actively engages in the capstone project and leverages feedback to refine technical and professional skills.
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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