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Medpace

Global CRO delivering full-service clinical trials

Project Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeLeuven, BelgiumNo salary listed

About the Job

Requirements

  • A Bachelor's degree in life sciences, such as Biomedical Sciences, is required.
  • Excellent computer skills, including word processing, databases, Excel, and Windows, are required.
  • Organizational and communication skills are required.

Responsibilities

  • Maintain study-related documents.
  • Attend study team calls.
  • Serve as the primary point of contact for study teams and investigational sites.
  • Prepare study metrics.
  • Ensure all aspects of designated clinical protocols comply with project timelines, budgets, and performance quality requirements.
  • Coordinate laboratory shipments.
  • Compose and maintain departmental operating procedures and work instructions.
  • Interact with Project Managers, Sponsors, and vendors on project-related issues.

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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