Trial Strategy & Delivery (TSD) Intern

GenmabPrinceton, FL
11dHybrid

About The Position

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 Trial Strategy & Delivery (TSD) 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 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 Genmab’s 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, you’ll 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.

Requirements

  • Pursuing a Master’s or advanced Bachelor’s 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.

Nice To Haves

  • 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 .

Responsibilities

  • Clinical Trial Systems and Process Optimization Support enhancements to Genmab’s 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.
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