Monitor progress of clinical studies at sites per protocol, SOPs, ICH-GCP.
Coordinate setup and monitoring: identify investigators and regulatory submissions.
Remote Hungary role with travel to sites for monitoring.
Work in a small CRO with influence and direct line management.
Travel up to 50-60% (domestic; some international).
Focus on quality, risk mitigation and cross-functional collaboration.

🎯 Requirements

Life science degree or equivalent experience.
2+ years as a CRA in CRO/pharma or biotech.
Domestic travel availability; international travel may be required.
Fluency in English and Hungarian.
Oncology monitoring experience a plus.
Study start-up activities experience preferred.

🎁 Benefits

Remote role in Hungary with site visits.
Reasonable travel and good work-life balance.
Opportunity to influence in a smaller CRO.
Supportive direct line management.

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