Clinical Data Manager Intern

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

Job Title

Clinical Data Manager Intern

Why Genmab

Our internship program provides interns with hands-on experience and relevant projects that directly align with our company's goals. Additionally, we believe our program provides a valuable opportunity to learn, thrive, and build a strong network. We encourage you to review our website to learn why we're always looking for smart, purpose-led candidates to play a role in our bold, extra[not]ordinary® future.

Job Overview

The Clinical Data Manager Intern will support Genmab's drug development efforts by gaining hands-on experience in clinical data management activities during a 10-week summer internship. This role offers exposure to select data management activities during the planning, start-up, conduct and closure of clinical trials. The Clinical Data Manager Intern will gain understanding of core DM deliverables such as EDC setup, data collection, validation of data in the clinical database, through practical assignments and mentorship. In this role the CDM Intern will also contribute to continuous process improvement in DM through suggestions and delivering on assigned tasks.

The intern will work closely with cross-functional teams, contributing to process improvements, EDC development and other projects that demonstrate tangible impact on drug developments.

What You'll Do

• Contribute to meetings within the data management group
• Shadow vendor oversight related to key deliverables e.g. eCRF design development, review of the eCRF completion guide, UAT, approve eCRF go live, Data management plan, Data validation plan, Data cleaning activities
• Evaluate trends in DM raised queries, ensuring data quality
• Proactively identify risks management related to data management activities in relation to trial conduct
• Review and provide input to protocol and amendment development
• Attend clinical trial team meetings as required
• Support timely development, update and maintenance of dashboards, if applicable

• 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.

• 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.

• You are genuinely passionate about our purpose
• You bring precision and excellence to all that you do
• You believe in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds
• You take pride in enabling the best work of others on the team
• You can grapple with the unknown and be innovative
• You have experience working in a fast-growing, dynamic company (or a strong desire to)
• You work hard and are not afraid to have a little fun while you do so!