Description

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 Research Scientist 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 Research Scientist (CRS) Intern supports Genmab's drug development efforts by gaining hands-on experience in clinical research science within the Clinical Strategy Team (CST) during a 10-week summer internship. This internship offers exposure to the role of clinical scientist and oncology clinical trials through practical assignments and mentorship. The intern will work closely with other CST members, as well as within cross-functional teams, contributing to ongoing clinical trial-related activities in order to provide high-quality and timely deliverables.

What You'll Do

• Works in collaboration with other Clinical Research Scientists
  
• Assists in supporting CRS team members in executing the clinical trial in alignment with the clinical development plan (CDP)
  
• May assist Sr. level CRS with the development of a trial protocol and to other study-related documents
  
• Exposure and education on performing ongoing data review, and summarizing efficacy and safety data for interpretation/analysis
  
• Participate in mentorship meetings and contribute to team discussions on process improvements and best practices.
  
• Provide general administrative support to the Global CRS team.
  
• Assist with the organization and planning of relevant team meetings for the Global CRS Team, and CRS leaders including generating agendas, meeting logistics, developing meeting minutes/action items and archiving.
  
• Assist with internal coordination of activities related to the CRS role in support of clinical trials.
  
• Provide support with the oversight and maintenance of Global CRS Team folder structure and coordination with relevant stakeholders.
  
• Assist with tracking progress across multiple initiatives, workstreams, and programs including communication to CRS and internal stakeholders as requested.
  
• Assist with the management and filing of medical-responsible regulatory documents in the eTMF adhering to required indexing administration with routine review for clinical trial completeness.
  
• Provide support for inspection readiness by contributing to the establishment, tracking, maintenance, and quality control of the medical-responsible regulatory documents in the eTMF.
  
• Conduct scientific research for publication or indication searches.
  
• Create, edit and quality check word documents, templates, PowerPoint presentations, and Excel worksheets.
  
• Ad-hoc task/projects as assigned.
  

Required Qualifications, Capabilities and Skills

• Candidate for PhD, Pharm D, MS or BS degree within the medical, biological, pharmaceutical science or related discipline
  
• Basic understanding of clinical research
  
• 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.
  
• Maintains attention to detail and quality in all deliverables while managing multiple tasks.
  
• Actively engages with CRS team members while leveraging their feedback
  

General Intern Information - Date/Location/Schedule

Internships will take place June - August 2026. 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.

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 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 you're 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, 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 LinkedIn and X.

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).