Trial Master File Intern
Genmab
Princeton, NJ0–27 yrs1h agovia LinkedIn
This job at a glance
- Who can apply
- New grads and up to 27 years · Bachelor's degree
- Must know
- OperationsData analysisExcelMicrosoft Office
- Nice to have
- Patient care
- Work
- On-site in Princeton · internship
- Pay
- Not stated by the employer.
- Skill demand
- Microsoft Office45%Excel44%Operations36%Data analysis7%of 99 similar entry-level jobs posted in the US this week
- Listed
- Nov 10, 2026 · still open
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About the Role
The Trial Master File Intern will support Genmab’s drug development efforts, gaining hands-on experience with the process and computerized systems used to manage clinical trial records that are critical to successful submission and approval of our medicines. This 10-week summer internship will provide opportunities to gain skills related to clinical trial site engagement and oversight of the clinical trial master file.
What You'll Do
- Assist with projects to improve business processes in TMF Operations, which can include writing or revising procedures, and updating templates and tools (e.g. the TMF Index).
- Participate in system enhancement projects, including software assessment and testing.
- Support with report development, trend and data analysis.
Requirements & Tech Stack
- Currently pursuing a Bachelor's in Life Sciences, Public Health, Data Science, or a related field.
- Strong Microsoft Applications skills (e.g., Word, Excel, and PowerPoint).
- Strong analytical skills with experience using Excel or other spreadsheet tools for data analysis and comparison.
- Strong computer skills and ability to learn technical applications in a fast-paced environment.
- Strong problem-solving abilities.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a collaborative team.
- High attention to detail and commitment to quality work.
Preferred Qualifications
- Comfortable synthesizing qualitative and quantitative data into clear summaries or reports.
- Familiarity with clinical trial processes or a general understanding of regulatory documentation is a plus.
General Intern Information
- Duration: 10 weeks, June – August 2027.
- Location: Princeton, NJ.
- Schedule: Required hybrid schedule (3 days in office, 2 days remote per week).
- Visa Sponsorship: This role is not eligible for work visa sponsorship.