Clinical Data Manager Intern

Genmab • Princeton, FL

5d • Hybrid

About The Position

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 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 d eliverables 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.

Requirements

• 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.

Nice To Haves

• 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.

Responsibilities

• 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

What This Job Offers

• Career Level: Intern
• Number of Employees: 1,001-5,000 employees