Trial Strategy & Delivery (TSD) 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

Trial Strategy & Delivery (TSD) 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

As a Trial Strategy & Delivery (TSD) Intern you will gain hands-on exposure to clinical trial planning operations and delivery. You will contribute to projects that strengthen Genmabs clinical trial execution capabilities through process improvement data-driven insights and operational excellence. Working cross-functionally with experts in Clinical Operations Data Analytics and Trial Planning youll apply both scientific and technical skills to enhance clinical trial efficiency and execution.

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 Youll Do

Interns will contribute to one or more of the following initiatives:

• Clinical Trial Systems and Process Optimization
  Support enhancements to Genmabs suite of operational software or contribute to building new tools including requirements gathering testing and process documentation.

• Operational Data and Metrics
  Develop tools and templates in Excel SharePoint and MS Project to automate tracking of study timelines resource metrics and deliverables.

• Regulatory and Quality Documentation
  Assist in maintaining high-quality documentation and compliance tracking aligned with regulatory standards using systems such as Veeva Vault or Box.

• Cross-Functional Collaboration
  Partner with the broader Development Operations Regulatory Affairs and Portfolio and Project Management teams to streamline data flow and ensure consistency across systems and study teams.

• Analytical Support and Insights
  Contribute to the design and delivery of data analyses for key performance metrics supporting decision-making in clinical trial planning and execution.

Required Qualifications Capabilities and Skills

• Pursuing a Masters or advanced Bachelors degree in Life Sciences Biomedical Engineering Regulatory Affairs or a related discipline.

• Strong analytical and organizational skills with proficiency in Microsoft Office Suite (Excel Word PowerPoint SharePoint).

• Demonstrated ability to manage data documentation or process improvement projects.

• Excellent communication teamwork and problem-solving skills.

Preferred Qualifications Capabilities and Skills

• Experience with Planisware Veeva Vault or other trial management systems.

• Background in clinical operations regulatory affairs or medical technology research.

• Familiarity with data analysis tools (e.g. R Python Tableau) and process automation.

• Exposure to market research or regulatory submission processes.

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.

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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