Clinical Research Associate

We are currently looking for a Clinical Research Associate (CRA) to support ongoing clinical trials across Belgium. This role is well suited to a CRA with around 2–3 years of monitoring experience who is looking to further develop their skills in a hands-on, collaborative environment.

• Perform Site Initiation Visits (SIVs), Site Monitoring Visits (SMVs), and Close-Out Visits (COVs) for IMP clinical trials
• Ensure sites are compliant with ICH-GCP, protocol requirements, and applicable regulations
• Maintain strong relationships with investigational sites and study teams
• Support accurate and timely documentation and reporting
• Travel primarily within Belgium and, with occasional visits to other countries
• Attend the office at least one day per week to support collaboration with the wider team

Experience

• 2–3 years of experience as a CRA with hands-on monitoring responsibilities
• Experience across all monitoring visits
• Native-level Dutch or French, with at least conversational ability in the other language
• Willingness to travel for monitoring visits (average 3–5 visits per month)
• Strong organisational skills and a proactive, collaborative mindset