Monitor progress of clinical studies at investigative sites per protocol and ICH-GCP.
Ensure studies are conducted, recorded, and reported per SOPs and regulations.
Coordinate study setup and monitoring (identify investigators, regulatory submissions, visits).
Travel up to 50-60% as required (domestic).

🎯 Requirements

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

🎁 Benefits

Remote-based position with site travel.
Small CRO with close management support.
Strong work-life balance and impact.
Inclusive culture with growth opportunities.
Please apply in English.

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