About this role
About the Role Clinical Research Associate II at ICON supports sponsor-driven cardio and obesity trials, designing and analyzing clinical trials and interpreting complex medical data to advance innovative treatments. This role is based in Miami, FL. 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 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 a range of benefits designed to support well-being and work-life balance.
- Various annual leave entitlements and health insurance offerings.
- Retirement planning options and LifeWorks global employee assistance program.
- Flexible country-specific benefits and additional perks such as childcare vouchers, gym discounts, travel subsidies, and health assessments.
- ICON emphasizes inclusion and equal opportunity in the workplace.