Intern - Regulatory Affairs

Labcorp
Baltimore, Maryland, United StatesPosted Sep 11, 2026

About the role

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Regulatory Affairs Intern to join our Regulatory Team located in Baltimore, MD!

Work Schedule: 40hrs per week

Job Responsibilities

Review scientific literature review protocols, confirm processes and data sources. Execute literature reviews using scientific databases to identify relevant information about the NGS (Next Generation Sequencing) market, similar medical devices, competing technologies and other topics that will help PGDx identify new requirements and enhancements to ensure our NGS products remain state-of-the-art. Research genetic variants that could become clinically significant for therapies that will help treat cancer patients, as they relate to PGDx products. The Regulatory Affairs intern will research requirements and processes to submit information about PGDx’s products to ethical committees and competent authorities to support clinical trials in the European Union. Become familiar with NGS technology, as well as US and global medical device requirements. Participate in regulatory body submissions and/or post-market surveillance data reporting. Perform

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