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
Clinical trial site monitoring
Adherence to protocols and GCP
Site performance assessment
Data collection and reporting
Site staff training and guidance
Stakeholder relationship management
Nice-to-have
Fostering inclusive environment
Driving innovation and excellence
Shaping future of clinical development
World's largest clinical research organization
Partnering with premier Biopharmaceutical companies
Key Requirements
Advanced degree in life sciences, nursing, or medicine