Site qualification, initiation, monitoring, close-out
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies
Job Summary
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Key responsibilities include conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
Matching Summary
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
Clinical trial monitoring experience
ICH-GCP guidelines knowledge
Site qualification, initiation, monitoring, close-out
Nice-to-have
Collaborative work environment
Fast-paced environment adaptability
Inclusive and diverse culture
Key Requirements
Bachelor's degree in scientific or healthcare field