Clinical Research Associate I/ Clinical Research Associate II

📋 Description

• 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
• 1 year 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
• Team player

🎁 Benefits

• Lower than average number of protocols, setting you up to be a protocol expert
• Reasonable travel, supporting work/life balance
• Voice will be heard in a smaller CRO with influence and impact
• Support from direct line management
• High CRA retention rates compared to industry averages