Monitor and own progress of clinical studies at investigative sites to ensure studies are
Coordinate activities to set up and monitor a study (identify investigators; help with regulatory
Join a smaller CRO with opportunities for influence and growth; travel is reasonable and work-life

🎯 Requirements

Graduate or postgraduate degree in a scientific or healthcare discipline
At least one year as a CRA in CRO/pharma/biotech or equivalent; site management experience preferred
Excellent communication and organizational skills; team player; client-focused
Willingness for domestic travel up to ~50-60% (international travel may be required for some senior
Fluency in English and German; experience in oncology

🎁 Benefits

Opportunity to contribute to oncology and rare disease trials in a precision medicine CRO
Support from direct line management; voice heard; strong retention culture

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