Global Medical Affairs Strategy, Multi-Indication Solid Tumors Intern
Genmab
Summary
The Global Medical Affairs Strategy, Multi-Indication Solid Tumors Intern will support strategic and operational activities within the Global Medical Affairs Strategy team across Genmab's multi-indication solid tumor portfolio. The intern will gain hands-on experience in launch readiness planning, advisory board operations, congress planning, scientific engagement tracking, knowledge management, and cross-functional coordination. This role offers exposure to global medical strategy and operational excellence initiatives supporting both pipeline and late-stage oncology assets.
Job description
Job Overview
The Global Medical Affairs Strategy, Multi-Indication Solid Tumors Intern will support strategic and operational activities within the Global Medical Affairs Strategy team across Genmab's multi-indication solid tumor portfolio. The intern will gain hands-on experience in launch readiness planning, advisory board operations, congress planning, scientific engagement tracking, knowledge management, and cross-functional coordination. This role offers exposure to global medical strategy and operational excellence initiatives supporting both pipeline and late-stage oncology assets.
What You'll Do
- Support Medical Affairs launch readiness activities by maintaining project plans, tracking key deliverables, and coordinating cross-functional follow-up actions.
- Assist with planning and execution of advisory boards, including agenda development, meeting logistics, contracts and attendee tracking, and post-meeting documentation.
- Maintain and enhance scientific engagement trackers and dashboards to support visibility of medical activities and key stakeholder interactions.
- Support medical congress planning activities, including timeline management, meeting preparation, logistics coordination, and execution support.
- Review, organize, and update Medical Affairs knowledge repositories, including SharePoint sites, to improve document accessibility and information management.
- Assist with development and standardization of contracting templates, tracking tools, and operational workflows.
- Create reports, summaries, presentation materials, and meeting documentation to support portfolio planning and operational decision-making.
- Analyze operational processes and identify opportunities to improve efficiency, organization, and knowledge sharing across the Medical Affairs organization.
- Present a final internship project summarizing key contributions, findings, and recommendations to Medical Affairs leadership.
Required Qualifications, Capabilities And Skills
- Currently enrolled in a PharmD or PhD degree program in Life Sciences, Healthcare Administration, Business, Public Health, Pharmacy, Biomedical Sciences, or a related field.
- Strong proficiency in Microsoft Office applications, particularly Excel, PowerPoint, Word, Teams, and SharePoint.
- Experience managing multiple projects, timelines, and priorities in a structured environment through academic, internship, or extracurricular activities.
- Demonstrated ability to organize, analyze, and maintain complex information and datasets with high attention to detail.
- Strong written and verbal communication skills with the ability to develop professional presentations, meeting documentation, and project summaries.
- Ability to work with confidential business information and maintain accuracy in operational tracking and documentation.
- Interest in biopharmaceutical drug development, Medical Affairs, oncology, and launch planning.
- Strong analytical and problem-solving skills with the ability to identify process improvement opportunities.
Preferred Qualifications, Capabilities And Skills
- Previous internship, research, or project experience within biotechnology, pharmaceutical, healthcare, consulting, or related industries.
- Familiarity with scientific engagement processes, advisory boards, or healthcare professional interactions.
- Experience working with project management, collaboration, or workflow management tools.
- Exposure to SharePoint administration, knowledge management systems, or document management platforms.
- Experience creating dashboards, trackers, or reports using Excel or other data visualization tools.
- Coursework in healthcare management, pharmaceutical sciences, biotechnology, business strategy, or project management.
- Interest in oncology and commercialization or launch planning within the biopharmaceutical industry.
- Demonstrated experience coordinating events, meetings, or stakeholder engagement activities.
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.
Requirements
- Currently enrolled in a PharmD or PhD degree program in Life Sciences, Healthcare Administration, Business, Public Health, Pharmacy, Biomedical Sciences, or a related field
- Strong proficiency in Microsoft Office applications, particularly Excel, PowerPoint, Word, Teams, and SharePoint
- Experience managing multiple projects, timelines, and priorities in a structured environment through academic, internship, or extracurricular activities
- Demonstrated ability to organize, analyze, and maintain complex information and datasets with high attention to detail
- Strong written and verbal communication skills with the ability to develop professional presentations, meeting documentation, and project summaries
- Ability to work with confidential business information and maintain accuracy in operational tracking and documentation
- Interest in biopharmaceutical drug development, Medical Affairs, oncology, and launch planning
- Strong analytical and problem-solving skills with the ability to identify process improvement opportunities
- Previous internship, research, or project experience within biotechnology, pharmaceutical, healthcare, consulting, or related industries
- Familiarity with scientific engagement processes, advisory boards, or healthcare professional interactions
- Experience working with project management, collaboration, or workflow management tools
- Exposure to SharePoint administration, knowledge management systems, or document management platforms
- Experience creating dashboards, trackers, or reports using Excel or other data visualization tools
- Coursework in healthcare management, pharmaceutical sciences, biotechnology, business strategy, or project management
- Interest in oncology and commercialization or launch planning within the biopharmaceutical industry
- Demonstrated experience coordinating events, meetings, or stakeholder engagement activities
Company overview
Genmab is a leading international biotechnology company headquartered in Copenhagen, Denmark, specializing in the development and commercialization of differentiated antibody therapeutics for the treatment of cancer. Founded in 1999, the company has established itself as a pioneer in antibody technology with its proprietary DuoBody, HexaBody, and DuoHexaBody platforms. Genmab's innovative approach focuses on creating next-generation antibody-based therapies that target specific cancer cells while minimizing damage to healthy tissues. The company has several marketed products including DARZALEX (daratumumab) for multiple myeloma, which has become a cornerstone treatment in hematological malignancies. Genmab's pipeline includes numerous clinical-stage candidates targeting various cancers, leveraging its expertise in antibody engineering to develop novel immunotherapies. The company collaborates with major pharmaceutical partners worldwide and maintains a strong commitment to advancing cancer treatment through cutting-edge science and patient-focused innovation.