CRA II

Join ICON plc as a CRA II to design and analyze clinical trials, interpreting complex medical data and contributing to the advancement of innovative treatments and therapies.

Requirements

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Benefits

• Annual leave entitlements
• Health insurance offerings
• Retirement planning offerings
• Employee Assistance Programme
• Life assurance