As a Clinical Research Associate 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 Clinical Research Associate 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 Clinical Research Associate 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
Protocol compliance
Data integrity
Patient safety
ICH-GCP guidelines
Nice-to-have
Innovative treatments and therapies
Collaborative work environment
Well-being and work life balance
Key Requirements
Bachelor's degree in scientific or healthcare field