Program Management Intern

Job Overview

The Program Management (PM) team plays a central role in advancing Genmab's drug development portfolio by supporting cross-functional program execution, project planning, and strategic decision-making. This Summer Intern role will provide insight into strategic program planning, governance processes, and operational excellence within a dynamic biotech company.

What You'll Do

As an intern, you will work alongside Program Managers (PMs) to support the execution of drug development programs by:

• Assisting in the development and tracking of project timelines, deliverables, and key milestones across cross-functional teams.
• Supporting the facilitation of program team meetings, including agenda preparation, meeting minutes, and action item follow-ups.
• Supporting cross-functional coordination and communication with core and sub-teams.
• Collaborating with project teams to gather and analyze program data, ensuring alignment with development strategy and goals.
• Contributing to the creation of presentation materials and reports for senior leadership and governance committees.
• Assisting in process improvement initiatives to enhance operational efficiency, team collaboration, and other Project Management tools and best practices.
• Gaining exposure to program governance, decision-making frameworks, and drug development processes from early to late-stage development.

Required Qualifications, Capabilities And Skills

• Currently enrolled in a Bachelor's or Master's program in Life Sciences, Pharmacy, Business, Healthcare Management, or a related field.
• Strong organizational skills and attention to detail.
• Ability to work effectively both independently and in a team setting.
• Excellent written and verbal communication skills.
• Strong problem-solving and critical-thinking abilities.
• Interest in drug development, and/or program management.

Preferred Qualifications, Capabilities And Skills

• Familiarity with Microsoft Office (MS Project, Excel, PowerPoint, Outlook, Teams).
• Previous experience or coursework in project management, clinical research, or some aspect of drug development is a plus.
• Some understanding of biopharmaceutical industry processes (e.g., clinical development phases, CMC, regulatory pathways, etc.) is a plus.

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.