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 conducting site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety throughout clinical trials.
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 site monitoring
Protocol compliance and data integrity
Oncology/Immunology therapeutic area
International and domestic travel
ICH-GCP guidelines knowledge
Nice-to-have
Strong organizational skills
Effective communication skills
Ability to work independently and collaboratively
Attention to detail
Inclusive and diverse work culture
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 3 years Clinical Research Associate experience