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.
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance.
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
protocol compliance
data integrity
patient safety
site collaboration
data review and query resolution
Nice-to-have
fostering an inclusive environment
driving innovation and excellence
advancement of innovative treatments
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Ability to work independently and collaboratively
Willingness to travel as required (approximately 60%)