CRA (Level I)

Take on the role of Clinical Research Associate I and support clinical trial monitoring and site management in Italy. Coordinate on-site and remote activities, ensuring protocol compliance and participant safety. Ideal for candidates with a scientific background and clinical research experience.

Skills

• clinical trial monitoring
• ich-gcp compliance
• risk-based monitoring
• source data review
• source data verification
• case report form review
• site compliance assessment
• clinical trial documentation
• clinical trial management system
• investigator site management
• regulatory compliance
• problem solving
• root cause analysis
• medical terminology
• clinical research
• therapeutic area knowledge
• process improvement
• stakeholder communication
• project reporting
• investigator site initiation
• investigator site close-out