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
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.
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 I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
Skills & Requirements
Must-have
Deliver high-quality clinical trial monitoring
Coordinate study setup and monitoring
Maintain study documentation accurately
Ensure patient safety and compliance
Develop strong stakeholder relationships
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Contribute to shaping the future of development
Key Requirements
University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines
Expertise to review and evaluate medical data
Excellent written and verbal communication in English