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Medpace

Global CRO delivering full-service clinical trials

Quality Assurance - Associate

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Life Sciences or a related field.
  • Experience conducting and supporting regulatory inspections is a plus.
  • Experience supporting or conducting audits.
  • Experience with a wide range of computerized systems.
  • Strong communication skills and a strong quality mindset.
  • Excellent written and verbal communication skills in English.
  • Ability to think and plan independently.
  • Good time management skills.
  • Ability to switch between a big-picture view and attention to detail.
  • Ability to work both on a team and independently.

Responsibilities

  • Facilitate Medpace sponsor audits onsite.
  • Review and assess responses to sponsor audit reports.
  • Provide clarity on the Quality Management System during sponsor audits and other external audits.
  • Provide guidance to Medpace study teams during sponsor audits.
  • Manage pre-inspection activities for Medpace inspections.
  • Provide inspection data trends to the Quality Metrics group for executive management review.
  • Manage the inspection backroom during regulatory inspections to facilitate timely delivery of requested documents.
  • Conduct mock interviews for subject matter experts during inspection preparation.
  • Review and analyze regulatory inspection data issued by regulatory authorities, including MHRA, EMA, and FDA.
  • Manage inspection-readiness training for Medpace stakeholders.
  • Conduct inspection-readiness visits at selected sites, as applicable, to assess inspection risk.
  • Act as the QA lead for inspections at Medpace.
  • Provide support as needed for inspections at Medpace external clients, including sponsors and investigator sites.
  • Maintain the repository memorializing frequently asked questions for regulatory inspections.

Desired Qualifications

  • Experience conducting and supporting regulatory inspections, including FDA, MHRA, and EMA inspections, is a plus.

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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