Monitor studies at investigative sites and ensure protocol/ICH-GCP compliance.
Coordinate site setup and monitoring (investigators, regulatory submissions, visits).
Remote-based role with travel to sites.

🎯 Requirements

Life science degree or equivalent experience.
2+ years as a CRA in CRO or pharma/biotech.
Domestic travel up to 50-60%; some international travel may be required.
Excellent communication and organizational skills; team player.
Fluency in English and Dutch; French a plus; oncology monitoring experience a plus.

🎁 Benefits

Remote-based role with travel to sites.
Impactful work in a smaller CRO with hands-on ownership.
Growth and development opportunities within the team.

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