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
Coordinate all necessary activities required to set up and monitor a study (i.e., identify

🎯 Requirements

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
Site management or equivalent experience in clinical research
Experience managing oncology studies
Excellent communication and organizational skills are essential. A team player
Evidence of a client focused approach

🎁 Benefits

Lower than average number of protocols
Reasonable travel, beneficial work/life balance
Support from direct line management

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