monitor and own the progress of clinical studies at investigative sites
ensure that 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 (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)

Life science degree and / or equivalent experience
2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent
Availability for domestic travel including overnight stays, as required
Excellent communication and organizational skills are essential. A team player.
Evidence of a client focused approach
Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
Fluency in English and Hungarian
oncology monitoring experience will be a plus

Clinical Research Associate II

Key skills