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Medpace

Global CRO delivering full-service clinical trials

Experienced Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in BelgiumNo salary listedRemote

About the Job

Requirements

  • A Bachelor of Science degree in a health-related field is required.
  • Previous experience as a clinical research associate is required.
  • Broad knowledge of medical terminology and clinical patient management is required.
  • Basic knowledge of drug therapy techniques and clinical research methodologies is required.
  • Excellent command of Dutch, English, and French is required.

Responsibilities

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites.
  • Perform source document verification and case report form review.
  • Perform regulatory document review.
  • Conduct study drug inventory.
  • Perform adverse event and serious adverse event reporting and follow-up.
  • Assess patient recruitment and retention.

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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