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

🎯 Requirements

Life science degree and/or equivalent experience
2 years or more as a CRA in a CRO or pharmaceutical/biotech industry or equivalent experience
Site management or equivalent experience in clinical research
Experience managing oncology studies
Excellent communication and organizational skills
Team player

🎁 Benefits

Lower than average number of protocols
Reasonable travel and work/life balance benefit
Influence and impact
Support from direct line management
High CRA retention rates compared to industry averages

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