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Medpace is seeking an office-based QA intern for Summer 2027 in Cincinnati, OH. You will assist with documentation, audit readiness, and QA data review, collaborating with QA staff and other departments to drive quality improvements.
The role supports the QA team in maintaining regulatory and quality management standards while providing hands-on exposure to clinical quality assurance processes and documentation practices.
Our corporate activities are growing rapidly, and we are currently seeking an office-based intern to join our Quality Assurance (QA) team for the Summer 2027 semester.
The Quality Assurance (QA) team focuses on ensuring the Medpace commitment to high ethical standards and compliance with regulatory and quality management system standards is maintained.
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.