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Genmab · 1 week ago

Clinical Research Scientist Intern

Princeton, NJ

Internship

Hybrid

Intern

Start in 2026 Summer

Genmab is an international biotechnology company dedicated to improving the lives of patients through innovative antibody therapeutics. The Clinical Research Scientist Intern will support drug development efforts by gaining hands-on experience in clinical research science and contributing to ongoing clinical trial-related activities within the Clinical Strategy Team.

BiotechnologyHealth CareManufacturingMedical

Culture & Values

No H1B

Responsibilities

Works in collaboration with other Clinical Research Scientists

Assists in supporting CRS team members in executing the clinical trial in alignment with the clinical development plan (CDP)

May assist Sr. level CRS with the development of a trial protocol and to other study-related documents

Exposure and education on performing ongoing data review, and summarizing efficacy and safety data for interpretation/analysis

Participate in mentorship meetings and contribute to team discussions on process improvements and best practices

Provide general administrative support to the Global CRS team

Assist with the organization and planning of relevant team meetings for the Global CRS Team, and CRS leaders including generating agendas, meeting logistics, developing meeting minutes/action items and archiving

Assist with internal coordination of activities related to the CRS role in support of clinical trials

Provide support with the oversight and maintenance of Global CRS Team folder structure and coordination with relevant stakeholders

Assist with tracking progress across multiple initiatives, workstreams, and programs including communication to CRS and internal stakeholders as requested

Assist with the management and filing of medical-responsible regulatory documents in the eTMF adhering to required indexing administration with routine review for clinical trial completeness

Provide support for inspection readiness by contributing to the establishment, tracking, maintenance, and quality control of the medical-responsible regulatory documents in the eTMF

Conduct scientific research for publication or indication searches

Create, edit and quality check word documents, templates, PowerPoint presentations, and Excel worksheets

Ad-hoc task/projects as assigned