Clinical Research Associate, Sponsor Dedicated

As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. You will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials and ensure protocol compliance, data integrity, and patient safety throughout the trial process.

Requirements

• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 2 years of experience as a Clinical Research Associate
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Strong organizational and communication skills, with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment

Benefits

• Annual leave entitlements
• Health insurance offerings
• Retirement planning offerings
• Global Employee Assistance Programme
• Life assurance
• Flexible country-specific optional benefits