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 will conduct site visits, ensure protocol compliance, maintain data quality, and facilitate smooth study conduct while promoting operational excellence.
ICON offers competitive salaries 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
Clinical trial site monitoring
Protocol compliance and data integrity
Patient safety management
Electronic case report form verification
Site audit and inspection readiness
Travel up to 60% internationally and domestically
Nice-to-have
Operational and scientific excellence promotion
Collaboration with investigators and site staff
Implementation of new clinical technologies
Strong organizational and communication skills
Bilingual English and French communication
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years clinical research associate experience
In-depth knowledge of ICH-GCP guidelines
Valid driver’s license
Certification or equivalent qualification in nursing or life sciences
1 to 2 years clinical site monitoring experience
English communication skills with medical terminology proficiency