Job Description
We are currently looking for an In-House Clinical Research Associate to join a clinical operations team based in the Brussels region.
This is a full-time, office-based position supporting the coordination and management of clinical trial activities across different countries. The successful candidate will work closely with study teams and investigational sites to ensure clinical trials are conducted in compliance with GCP, SOPs, and applicable regulatory requirements.
Responsibilities
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Support the day-to-day coordination of clinical trial activities
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Assist with site management and communication with investigational sites
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Review and maintain essential trial documentation and Trial Master File (TMF/eTMF)
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Support collection and tracking of regulatory documents
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Ensure study documentation is complete, accurate, and inspection-ready
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Support study start-up, maintenance, and close-out activities
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Track study timelines, site activation status, and outstanding actions
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Support preparation for audits and inspections
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Maintain compliance with ICH-GCP guidelines and company SOPs
Requirements
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University degree in Life Sciences, Pharmacy, Biomedical Sciences, or related field
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Previous experience in clinical research, clinical operations, or study coordination
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Experience in an In-House CRA, CTA, or similar clinical support role is preferred
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Good understanding of clinical trial processes and GCP guidelines
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Strong organisational and communication skills
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Detail-oriented with the ability to manage multiple priorities
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Fluent in English and an additional European language
Working Conditions
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Full-time permanent position
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Office-based role in the Brussels region
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International environment
