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Entry-level Clinical Research Associate - Clinical Study Coordinator experience required

Leuven, Belgium💼 Full-time🗓 2026-09-29 → 2026-09-30

Core

Conduct on-site monitoring visits for clinical trials to ensure compliance with protocols and regulatory requirements for drug and medical device development.

Role type

Entry-level Clinical Research Associate (CRA)

Builds

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

Domain

Clinical research / Life sciences

Deliverable

client delivery

Required skills

Clinical research coordination, site monitoring, regulatory compliance (GCP/SOPs), medical record verification, adverse event reporting, patient recruitment assessment, inventory management

Preferred skills

Nursing, dietetics, pharmacy, biomedical research, or sales background

Technologies

Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), IWRS, Microsoft Office

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