Intern - Regulatory Affairs

Labcorp•Baltimore, MD

1d•$18 - $20•Onsite

About The Position

Labcorp is seeking a Regulatory Affairs Intern to join their Regulatory Team in Baltimore, MD. This internship is part of the Labcorp 2027 Global Internship Program, offering an 11-week paid experience focused on impactful projects and real-world exposure in healthcare innovation. The role involves working with the PGDx Regulatory and Quality Teams to ensure the suitability, safety, and effectiveness of next-generation sequencing (NGS) medical devices. Interns will gain exposure to Labcorp's global business, culture, and leadership through enterprise-wide learning, leadership interactions, an in-person intern event, senior leader speaker sessions, continuous networking opportunities, engagement with employee resource groups, and dedicated mentoring.

Requirements

Current enrollment in a Bachelor’s degree program in Biology, Biomedical Engineering, Public Health, Genetics or Regulatory.
Interested in genetics, biomedical engineering, cell biology, regulatory affairs and/or next generation sequencing technology
Demonstrate strong attention to detail
Eagerness to learn new skills and scientific concepts
Show initiative and the ability to work independently under general supervision
Maintains professionalism, including punctuality and appropriate conduct
Strong communication skills; both written and verbal
Actively participates in training sessions and applies newly learned skills accordingly
Looking for practical experience with US and global medical device quality and regulatory requirements
Can deliver results in an academic or professional setting.
Ability to collaborate with various stakeholders and internal/external colleagues.

Nice To Haves

Preferred candidates are rising juniors and seniors (Dec 2027 through June 2029 graduation) who are currently enrolled in a relevant degree program; however, all current students pursuing related studies are encouraged to apply.

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.
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 related duties as assigned by supervisor.
Maintain compliance with all company policies and procedures.