Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Job Summary
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.
Matching Summary
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Skills & Requirements
Must-have
Monitoring clinical trial sites
Ensure adherence to protocols
Conduct site visits
Collaborate with cross-functional teams
Provide training and guidance
Build effective relationships
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Shape the future of clinical development
Nurture talent
Focus on well-being and work-life balance
Key Requirements
Extensive experience as a Clinical Research Associate in Australia