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ICON is seeking a Clinical Research Associate II in Nanjing, China, to manage clinical trial activities, ensuring protocol compliance and data integrity. The ideal candidate will have a scientific background, at least two years of relevant experience, and strong communication skills.
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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 opportunities.
Matching Summary
Match Score: 75
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ICON is seeking a Clinical Research Associate II in Nanjing, China, to manage clinical trial activities, ensuring protocol compliance and data integrity. The ideal candidate will have a scientific background, at least two years of relevant experience, and strong communication skills.
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Skills & Requirements
Must-have
Clinical trial monitoring
Protocol compliance
Patient safety
ICH-GCP guidelines
Nice-to-have
Innovative treatments
Collaborative environment
Work-life balance
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years of experience as a Clinical Research Associate