Monitor clinical studies at investigative sites per protocol and ICH-GCP.
Coordinate study setup and monitoring: investigators, regulatory submissions, visits.
Remote-based with travel to sites for morning visits; based in Belgium/Netherlands.

🎯 Requirements

Life science degree or equivalent experience.
2+ years as a CRA in CRO or pharma; site management experience.
Domestic travel with overnight stays; international travel may be required.
Fluent in English and Dutch; French a plus; oncology monitoring experience a plus.
Study start-up activities experience preferred.

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