About this role
About the Role ICON is seeking a Clinical Research Associate II to support sponsor-dedicated monitoring for cardio and obesity trials in Miami, FL. The role focuses on designing and analyzing clinical trials, interpreting complex data, and ensuring safe and compliant study conduct. What You'll Do
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to preparation and review of study documents including protocols and clinical study reports What We're Looking For
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum 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 approximately 60%. Compensation & Benefits
- Competitive salary and a broad benefits package designed to support well-being and work-life balance.
- Various annual leave entitlements and a range of health insurance offerings.
- Competitive retirement planning options.
- Global Employee Assistance Programme with LifeWorks for 24/7 well-being support.
- Life assurance and flexible country-specific optional benefits (including childcare vouchers, travel passes, gym discounts, etc.).
ICON is committed to inclusion and belongs to a diverse, accessible workplace. All qualified applicants will receive equal consideration without regard to race, color, religion, sex, etc.