Trial Master File & Site Management Intern
Location: Princeton, New Jersey, USA (Hybrid: 3 days onsite, 2 days remote)
Category: Research & Discovery
Job ID: R14746
Internship Duration: June – August 2026
Overview
Genmab, a leading global biotechnology company, is seeking a Trial Master File & Site Management Intern to join its Site Management & Feasibility team. This internship offers hands-on experience in clinical trial site engagement, operational oversight, and Trial Master File (TMF) management.
Interns will collaborate with cross-functional teams across the US, Denmark, and the Netherlands, gaining exposure to global clinical operations, site performance tracking, and clinical trial governance processes. This internship is ideal for students pursuing Life Sciences, Public Health, Data Science, or related fields who are interested in clinical research operations and regulatory compliance.
Key Responsibilities
Trial Master File Management:
Ensure compliance of the TMF through validation and verification of accurate metadata.
Review “Note to File” entries to confirm proper TMF filing locations.
Support reporting trends and data analysis for clinical operations.
Site Management & Performance:
Create site performance reports using qualitative and quantitative data from key stakeholders.
Oversee operational site metrics, including timelines, enrollment, compliance, and database lock readiness.
Provide site status updates and actively participate in trial-related meetings.
Research & Analysis:
Evaluate clinical trial institutions and networks to identify capabilities and assess patient populations aligned with Genmab’s portfolio.
Synthesize data into actionable insights to support strategic site engagement.
Required Qualifications
Currently pursuing a Bachelor’s degree in Life Sciences, Public Health, Data Science, or a related field.
Strong Microsoft Office skills, including Word, Excel, and PowerPoint.
Analytical skills with experience in data analysis, reporting, and spreadsheet tools.
Strong computer literacy and the ability to learn technical applications quickly.
Excellent problem-solving, written, and verbal communication skills.
Ability to work independently and collaboratively within a global team.
High attention to detail and commitment to quality.
Ability to conduct literature or database research to identify healthcare institutions, networks, or population data.
Preferred Qualifications
Demonstrates a global mindset and adaptability to cross-cultural collaboration.
Interest in artificial intelligence, innovation, and technology-driven solutions.
Proactive, eager to learn, and capable of thriving in a fast-paced clinical environment.
Familiarity with clinical trial processes and regulatory documentation is a plus.
Comfortable synthesizing qualitative and quantitative data into clear reports or summaries.
Internship Details
Hybrid Work Schedule: 3 days onsite in Princeton, NJ; 2 days remote per week.
Eligibility: Open to undergraduate students; not eligible for visa sponsorship.
Mentorship & Development: Gain guidance from experienced clinical operations professionals and cross-functional teams.
Hands-On Exposure: Learn global TMF management, clinical site engagement, operational analytics, and clinical trial compliance.
About Genmab
Genmab is an international biotechnology company focused on improving patient outcomes through innovative antibody therapeutics, including bispecific T-cell engagers, antibody-drug conjugates, and next-generation immune checkpoint modulators.
With a global presence across North America, Europe, and Asia-Pacific, Genmab leverages translational, quantitative, and data sciences to advance cutting-edge therapies. By 2030, the company aims to revolutionize cancer and serious disease treatment with Knock-Your-Socks-Off (KYSO®) antibody medicines.
Learn more at Genmab.com.
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