About this role
About the Role ICON is seeking a Clinical Research Associate II to contribute to the design, monitoring and analysis of clinical trials, ensuring high-quality data and patient safety while supporting study delivery across sites. What You'll Do
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- 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 What We're Looking For
- 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.
- Willingness to travel as required (approximately 60%) Compensation & Benefits
- Competitive salary and benefits package.
- Various annual leave entitlements.
- Health insurance offerings to suit you and your family\'s needs.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global support network.
- Life assurance and flexible country-specific optional benefits (childcare vouchers, bike purchase schemes, gym discounts, travel passes, health assessments, and more). Industry Healthcare