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 monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards while supporting successful trial execution.
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
Good Clinical Practice (GCP) standards
Oncology/Haematology trial experience
Regulatory compliance in Australia
Site performance assessment
Clinical trial data collection
Valid driver’s license
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder relationship management
Problem-solving skills
Organizational skills
Communication and interpersonal skills
Ability to influence compliance
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive CRA experience with early Phase Oncology/Haematology trials
Strong understanding of Australian clinical trial regulations