ICON is seeking a Clinical Research Associate II in Sofia, Bulgaria, responsible for monitoring clinical trials and ensuring protocol compliance. The ideal candidate should have at least two years of relevant experience and a strong understanding of clinical trial processes
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.
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Matching Summary
Match Score: 85
ICON is seeking a Clinical Research Associate II in Sofia, Bulgaria, responsible for monitoring clinical trials and ensuring protocol compliance. The ideal candidate should have at least two years of relevant experience and a strong understanding of clinical trial processes.
Skills & Requirements
Must-have
clinical trial monitoring activities
protocol compliance
data integrity
patient safety
site qualification, initiation, monitoring, and close-out visits
Nice-to-have
foster an inclusive environment
driving innovation and excellence
advancement of innovative treatments and therapies
Key Requirements
Minimum of 2 years of experience as a Clinical Research Associate
Bachelor's degree in a scientific or healthcare-related field
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Willingness to travel as required (approximately 60%)