Monitor and own the progress of clinical studies at investigative sites
Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
Coordinate all necessary activities required to set up and monitor a study

Life science degree and / or equivalent experience
2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
Site management or equivalent experience in clinical research
Availability for domestic travel including overnight stays (international travel may be required for some senior level positions)
Excellent communication and organizational skills are essential
Evidence of a client focused approach
Fluency in English, Dutch
French will be a plus
Oncology monitoring experience will be a plus

Clinical Research Associate I/II

Key skills