Standards and Systems Intern

Genmab; Princeton (NJ); Hybrid; USD 25,000 - 39,000; Part time

Job summary

Genmab is offering a 10-week Standards and Systems Intern role in Princeton, NJ, with a hybrid schedule (3 days in office, 2 remote). The intern will gain hands-on experience in clinical data management, CRF design, edit checks, and data governance while collaborating with cross-functional teams to support Genmab’s drug development efforts.

Interns will work with the Standards & Systems team to understand regulatory requirements, contribute to process improvements, and complete assigned tasks

Qualifications

• Enrollment in a Bachelor or Master’s program in Health Sciences, Data Science, or a related field.
• Strong analytical and 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.
• Genuine interest in clinical research and drug development.

Responsibilities

• Contribute to meetings within the standards and systems group.
• Assist in intake, review, and documentation of Standards Change Requests.
• Participate in validation activities for CRFs and edit checks.
• Update and maintain the Genmab Standard CRF Template and AMU Guide.
• File standards and system documentation within eTMF and ensure inspection readiness.
• Process ServiceNow requests for EDC user access and monitor compliance.
• Maintain the Standards & Systems SharePoint site and ensure content is current.
• Attend standards and systems departmental meetings and study team meetings.
• Draft, update, and improve departmental process documents and workflows.

Skills

Analytical thinking

Communication skills

Team collaboration

Attention to detail

Interest in clinical research

Education

Bachelor's or Master's in Health Sciences or Data Science

Tools

Programming languages

Job description

Job Title

Standards and Systems Intern

Why Genmab

At Genmab, interns don’t just learn about the work - they help move it forward. Our internship program provides meaningful, hands-on experience through real projects that directly support our teams, business priorities, and mission to transform the lives of people with cancer and other serious diseases.

From day one, interns are welcomed as part of the team and given opportunities to contribute, collaborate, and make an impact. Along the way, you’ll learn from talented colleagues and senior leaders, build new skills, expand your professional network, and gain exposure to the innovative work happening across Genmab.

We’re always looking for smart, curious, purpose-led people who are ready to bring fresh perspectives and bold ideas. Explore our website to learn more about Genmab and how you could play a role in our bold, extra[not]ordinary® future.

Job Overview

The Standards and Systems Intern will support Genmab’s data standards, clinical systems, and standards governance activities by gaining hands-on experience in key components of clinical data management during a 10-week summer internship.

This role provides practical exposure to the foundational elements that ensure consistency, quality, and compliance in clinical data collection across Genmab trials. Working closely with the Standards & Systems team, the intern will develop an understanding of Genmab’s core standards requirements, including Case Report Form (CRF) design, edit check testing and validation, processing standards change request and Service Now Request related to EDC system user access, all through direct assignments and mentorship. The intern will also contribute to continuous process improvement initiatives by offering suggestions and completing assigned tasks that enhance departmental efficiency and quality.

In addition to supporting the Standards & Systems team, the intern will collaborate with cross-functional teams, contributing to process improvements, development activities, and other projects that have a tangible impact on Genmab’s drug development efforts.

What you’ll do

• Contribute to meetings within the standards and systems group
• Assist in the intake, review, and documentation of Standards Change Requests
• Participate in internal alignment discussions and cross-functional meetings related to implementation of standards
• Participate in validation activities for the build of standard Case Report Forms (CRFs) and edit checks
• Assist in updating and maintaining the Genmab Standard CRF Template and Allowable Modification and Usage (AMU) Guide
• Assist with filing standards and system documentation within eTMF, ensuring accuracy and inspection readiness
• Help process ServiceNow requests for EDC user access and monitor compliance with access-control procedures
• Maintain and update the Standards & Systems SharePoint site, ensuring that content is current, organized, and accessible
• Attend standards and systems departmental meetings and/or study team meetings as required
• Contribute to drafting, updating, and improving departmental process documents, workflows, and best-practice guides

Required qualifications, capabilities and skills

• Enrollment in a Bachelor or Master’s program in Health Sciences, Data Science, or a related field.
• Basic understanding of clinical trial regulatory environment.
• Strong analytical and 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.
• Genuine interest in clinical research and drug development.

Preferred qualifications, capabilities and skills

• Demonstrates initiative, a proactive attitude, and eagerness to learn in a fast-paced environment.
• Effectively communicates and collaborates with team members, mentors, and stakeholders.
• Applies academic expertise in open-source programming languages and adapts quickly to new tools and methodologies.
• Maintains attention to detail and quality in all deliverables while managing multiple tasks.
• Actively engages in the capstone project and leverages feedback to refine technical and professional skills.

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.

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.

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