Clinical Data Manager Intern

At Genmab we are dedicated to building extranotordinary 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 companys 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 were always looking for smart purpose-led candidates to play a role in our bold extranotordinary future.

Job Overview

The Clinical Data Manager Intern will support Genmabs 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 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 Youll 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 Masters 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.

Whats 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 its important to complete all relevant questions to ensure we have as much information about you as possible.

Every application matters to us and well carefully review each submission as quickly as possible to see if your qualifications align with the role. While were unable to provide individual updates rest assured that were working diligently to move through the process efficiently.

If you move forward in the process youll 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 youll 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 cant wait to see where this journey takes you!

About You

• You are genuinely passionate about our purpose

• You bring precision and excellence to all that you do

• You believe in our rooted-in-science approach to problem-solving

• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds

• You take pride in enabling the best work of others on the team

• You can grapple with the unknown and be innovative

• You have experience working in a fast-growing dynamic company (or a strong desire to)

• You work hard and are not afraid to have a little fun while you do so!

Locations

Genmab maximizes the efficiency of an agile working environment when possible for the betterment of employee work-life balance. Our offices are crafted as open community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether youre in one of our 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 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 Genmabs 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 and follow us on LinkedIn and X.

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