Clinical Trial Operations Intern

Job Overview

As a Clinical Trial Operations 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, Vendor Oversight and Standards, Clinical Data, Integration & Reporting, and Trial Planning, you'll apply both scientific and technical skills to enhance clinical trial efficiency and execution; documenting clinical operation practices that are consistent, scalable, and inspection ready.

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 You'll Do

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

• Process optimization and quality documentation: Contribute to designing compliant processes and assist in ensuring high-quality documentation aligned with regulatory standards.
• Business and clinical trial operations: Support enhancements and/or building new operational tools leveraging AI, PowerBI or other software, including requirements gathering, testing, and process documentation.
• Inspection readiness and trial documentation: Develop a practical readiness toolkit by reviewing trial documentation, identifying common gaps, and creating checklists or dashboards that support consistent, inspection-ready execution.
• Trial performance metrics and insights: Analyze operational data to identify trends, bottlenecks, and improvement opportunities, and develop clear visualizations or summaries for study teams and leadership.
• Knowledge management and digital enablement: Organize clinical operations guidance and lessons learned into accessible resources and explore responsible uses of automation or AI to improve information retrieval and team collaboration.

Required Qualifications, Capabilities And Skills

• Currently pursuing a Bachelor's degree (Junior or Senior standing) or Master's degree in Life Sciences, Biomedical Engineering, Drug Discovery and Development, or a related discipline
• Strong analytical and organizational skills with proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, SharePoint) and comfort with AI and/or PowerBI to solve complex problems.
• Demonstrated ability to manage data, documentation, or process improvement projects.
• Excellent communication, teamwork, and problem-solving skills.

Preferred Qualifications, Capabilities And Skills

• Experience using or classwork in Lean, Six Sigma and/or Project Management practices.
• Knowledge or experience in GxP practices or ICH guidelines.
• Experience with Planisware, Veeva Vault, or other trial management systems.
• Background in clinical operations, drug development, or medical technology research.

General Intern Information – Date/Location/Schedule

Internships will take place over 10 weeks from June – August 2027. 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. This role is not eligible for work visa sponsorship at the time of the application or in the future.