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Medpace

Global CRO delivering full-service clinical trials

Quality Assurance Intern

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Internship · Summer 2027Cincinnati, OH, USANo salary listed

About the Job

Requirements

  • Pursuing a Bachelor's degree or higher in Life Sciences or a similar field.
  • Available to work 40 hours a week onsite in Cincinnati, Ohio.
  • Have a GPA of 3.5 or higher.
  • Have internship or project experience with clinical quality assurance.
  • Be proficient in Microsoft Office, including Word, Excel, and Outlook.
  • Have strong attention to detail and organizational skills.

Responsibilities

  • Assist with quality system documentation and record management.
  • Support audit preparation and inspection readiness activities.
  • Help review and organize quality assurance data and reports, and support process improvements.
  • Participate in meetings and projects related to quality and compliance initiatives.
  • Collaborate with quality assurance staff and other departments as needed.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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