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.
As a Clinical Research Associate at ICON, you will monitor clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards while supporting site staff and maintaining effective relationships.
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
Monitoring clinical trial sites
Adherence to Good Clinical Practice standards
Managing multiple clinical trial sites
Proficiency in clinical trial software
Ability to travel at least 60% of the time
Valid driver’s license required
Nice-to-have
Strong organizational skills
Problem-solving skills
Excellent communication skills
Stakeholder management
Collaborative cross-functional teamwork
Training and guidance provision
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Experience as a Clinical Research Associate
Strong understanding of clinical trial processes and regulatory requirements
Ability to travel internationally and domestically 60% of the time