You will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Job Summary
You will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry 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
You will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Skills & Requirements
Must-have
Monitoring clinical trial sites
Adherence to study protocols
Regulatory requirements and GCP
Data integrity and participant safety
Site performance assessment
Training and guidance to site staff
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Shaping the future of clinical development
Building effective relationships with stakeholders
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate