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 trialsEnsure sites are compliant with ICH-GCP, protocol requirements, and applicable regulationsMaintain strong relationships with investigational sites and study teamsSupport accurate and timely documentation and reportingTravel primarily within Belgium and, with occasional visits to other countriesAttend 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 responsibilitiesExperience across all monitoring visitsNative-level Dutch or French, with at least conversational ability in the other languageWillingness to travel for monitoring visits (average 3–5 visits per month)Strong organisational skills and a proactive, collaborative mindset