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Virtual Event: From Clinical Research Coordinator to CRA

Leuven, Belgium💼 Full-time🗓 2026-09-14 → 2026-09-24

Core

Conducting qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with protocols and regulations.

Role type

Clinical Research Associate (CRA)

Builds

Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device development

Domain

Clinical Research / Life Sciences

Deliverable

client delivery

Required skills

Clinical trial monitoring, regulatory compliance (GCP/SOPs), site qualification, source data verification, adverse event reporting, patient recruitment assessment, cross-functional collaboration

Preferred skills

Medical or life science background, travel readiness (60-70%), driver's license

Technologies

Microsoft Office

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