ICON is seeking a Clinical Research Associate in Israel to contribute to clinical trial operations, emphasizing high-quality monitoring and collaboration with stakeholders. The ideal candidate should possess relevant clinical trial monitoring experience, a degree in a related field, and knowledge of ICH-GCP guidelines
Job Summary
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
In addition to your competitive salary, 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
Match Score: 85
ICON is seeking a Clinical Research Associate in Israel to contribute to clinical trial operations, emphasizing high-quality monitoring and collaboration with stakeholders. The ideal candidate should possess relevant clinical trial monitoring experience, a degree in a related field, and knowledge of ICH-GCP guidelines.
Skills & Requirements
Must-have
Clinical trial monitoring
ICH-GCP guidelines
Patient safety compliance
Study documentation maintenance
Stakeholder relationship management
Nice-to-have
Fostering inclusive environment
Driving innovation and excellence
Collaborative team delivery
Key Requirements
University degree in medicine, science, or equivalent
Excellent written and verbal communication in English