Trial Strategy & Delivery (TSD) Intern

Genmab • Princeton, TX

35d • Hybrid

About The Position

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.

What This Job Offers

• Career Level: Intern
• Number of Employees: 1,001-5,000 employees