Job Specifications
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 Title
Clinical Data Manager Intern
Why Genmab
Our internship program provides interns with hands-on experience and relevant projects that directly align with our company’s goals. Additionally, we believe our program provides a valuable opportunity to learn, thrive, and build a strong network. We encourage you to review our website to learn why we’re always looking for smart, purpose-led candidates to play a role in our bold, extra[not]ordinary® future.
Job Overview
The Clinical Data Manager Intern will support Genmab’s drug development efforts by gaining hands-on experience in clinical data management activities during a 10-week summer internship. This role offers exposure to select data management activities during the planning, start-up, conduct and closure of clinical trials. The Clinical Data Manager Intern will gain understanding of core DM deliverables such as EDC setup, data collection, validation of data in the clinical database, through practical assignments and mentorship. In this role the CDM Intern will also contribute to continuous process improvement in DM through suggestions and delivering on assigned tasks.
The intern will work closely with cross-functional teams, contributing to process improvements, EDC development and other projects that demonstrate tangible impact on drug developments.
What You’ll Do
Contribute to meetings within the data management group
Shadow vendor oversight related to key deliverables e.g. eCRF design development, review of the eCRF completion guide, UAT, approve eCRF go live, Data management plan, Data validation plan, Data cleaning activities
Evaluate trends in DM raised queries, ensuring data quality
Proactively identify risks management related to data management activities in relation to trial conduct
Review and provide input to protocol and amendment development
Attend clinical trial team meetings as required
Support timely development, update and maintenance of dashboards, if applicable
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/Schedule
Internships will take place June through August 2026 and be based in Princeton, NJ. This role will operate on a required hybrid schedule – 3 days in the office and 2 days remote per week. This role is not eligible for sponsorship.
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
About the Company
We are an international biotech company committed to our goal of improving the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, our passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational, quantitative, and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators, and effector function enhanced a...
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