ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
The role involves coordinating all activities for setting up and monitoring clinical studies, ensuring compliance with protocols and regulatory requirements, and maintaining study documentation.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Clinical trial monitoring experience
Knowledge of ICH-GCP guidelines
Study documentation management
Patient safety compliance
Travel availability at least 60%
Nice-to-have
Strong stakeholder collaboration
Excellent written and verbal communication
Good social skills for query resolution
Ability to work independently
Key Requirements
At least 2 years CRA monitoring experience
University degree in medicine, science, or equivalent
Valid driver’s license
Ability to travel internationally and domestically