Genmab

About the Company

We are an international biotech company committed to our goal of improving the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, our passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational, quantitative, and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators, and effector function enhanced antibodies. By 2030, our vision is to transform the lives of people with cancer and other serious diseases with knock-your-socks-off (KYSO(r)) antibody medicines. We are united by our core values: a passion for innovation, determination, integrity, and working as one team and respecting each other. When you work at Genmab you'll be part of a warm, fun, dynamic community seeking out and embracing the opportunity to build new and bold futures within a rapidly growing biotechnology company. Genmab is a place where you can be authentically you; you are empowered to innovate, build solutions and execute; you feel cared for and supported. In its totality, this makes working at Genmab an extra[not]ordinaryTM experience. Established in 1999, we are headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com.
Disclaimer: http://bit.ly/GENDisclaimer

Listed Jobs

Company Name

Genmab

Job Title

Clinical Data Manager Intern

Job Description

**Job title** Clinical Data Manager Intern **Role Summary** A 10‑week summer internship focused on clinical data management (DM) in drug development. The intern supports planning, startup, conduct, and close‑out of clinical trials, gaining hands‑on experience in electronic data capture (EDC) setup, eCRF design, data validation, and process improvement under mentorship. **Expectations** * Complete assigned DM tasks within deadlines, delivering high‑quality, detailed results. * Demonstrate initiative, curiosity, and the ability to work independently and collaboratively. * Engage actively in meetings, vendor oversight, and continuous improvement activities. **Key Responsibilities** * Attend data management group meetings and contribute to discussions. * Shadow vendor oversight for eCRF design, eCRF completion guide review, UAT, go‑live approval, data management plan, and data validation plan. * Monitor and analyze DM query trends to ensure data quality. * Identify and communicate risks associated with DM activities during trial conduct. * Review and provide input on protocol and amendment development. * Support clinical trial team meetings and assist in documentation. * Develop, update, and maintain dashboards for DM metrics. **Required Skills** * Strong analytical and problem‑solving capabilities. * Excellent written and verbal communication. * Attention to detail and commitment to quality. * Ability to work independently and in a team. * Basic understanding of clinical trial regulatory environment. * Proficiency in analyzing data sets and using spreadsheet tools. **Required Education & Certifications** * Enrolled in a Bachelor’s or Master’s program in Health Sciences, Data Science, or a related field. * No specific certifications required. ---

Princeton, United states

Hybrid

Fresher

07-01-2026