ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
The Clinical Research Associate II will independently monitor Phase II–IV clinical trials, manage multiple sites, and ensure protocol compliance and patient safety.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Monitor Phase II–IV clinical trials
Ensure compliance with ICH-GCP
Manage clinical studies in France
Conduct site qualification and monitoring visits
Collaborate with investigators and site staff
Perform data review and query resolution
Nice-to-have
Strong organizational skills
Problem-solving skills
Attention to detail
Fluency in French and English
Work in hybrid home or office setting
Contribute to study documentation preparation
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years CRA experience
Strong understanding of clinical trial processes
Knowledge of regulatory requirements within CRO or Pharma