Clinical Research Associate
On-site · Miami, Florida, United States
Job Summary
Clinical Research Associate II responsible for designing and monitoring clinical trials, performing site qualification/initiation/monitoring/close-out visits, ensuring protocol compliance and data integrity, collaborating with investigators and site staff, reviewing data and resolving queries, and contributing to study documentation such as protocols and clinical study reports. Requires Bachelor's degree in a scientific/healthcare field and at least 2 years of CRA experience, with ability to travel ~60% and be based in Miami, FL. ICON is an inclusive employer offering a comprehensive rewards package.
Required Qualifications
- 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%)
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.