Monitor clinical studies at investigative sites per protocol, SOPs, ICH-GCP, and regulations.
Coordinate study setup activities: identify investigators, regulatory submissions, pre-study and
Remote-based position focused on Belgium with some Netherlands site support.
Travel up to 50-60% may be required depending on seniority.
Work in a smaller CRO environment with direct line management support.

🎯 Requirements

Life science degree and/or equivalent experience.
At least 2 years as a CRA in CRO/pharma/biotech or equivalent.
Domestic travel availability, overnight stays may be required.
Excellent communication and organizational skills; client-focused; team player.
English and Dutch fluency; French a plus.

🎁 Benefits

Remote-based role with Belgium focus and potential Netherlands site support.
Competitive CRO-focused environment with growth opportunities.

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