Medpace Functional Areas
Quality Assurance
QA focuses on compliance to ensure safety of research participants and the integrity, quality, and reliability of data obtained from our clinical trials and labs.
QA focuses on compliance to ensure safety of research participants and the integrity, quality, and reliability of data obtained from our clinical trials and labs.
Key Positions
CRO QA
Primarily responsible for conducting Investigative Site Audits at Medpace sites globally. Auditors on this team act as the Quality Program Lead on clinical trials by supporting national and international regulatory standards (GCP) and guidance for pharmaceuticals, biologics and medical devices.
Laboratory QA
Supporting global Lab operations, Lab QA ensures compliance to SOPs, lab regulations and standards, and assists in the creating and maintenance of controlled documents for Medpace MRL & MBL.
Global Inspections & Sponsor Audit Management
The GISAM team is responsible for the management of sponsor audits and regulatory inspections, and facilitating the QA relationship with external clients.
Degrees, Qualities, and Competencies
What We Look For
We seek the best to be the best. A superb resumé is a good start, but there are other attributes we look for.
Related Degrees
A bachelor’s degree is required for most positions. Additional degree(s) and experience may be required for some positions.
Related Experience
1-2 years of experience in a pharmaceutical or CRO setting is preferred, but not required. Related experience isn’t required for entry-level positions.
Attention to Detail
Accomplish tasks while demonstrating a thorough concern for all the areas involved, no matter how small. This means monitoring and checking work or information while organizing time and resources efficiently.
Welcome to your future.
Find Your Fit
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