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ICON Clinical Research is seeking a Clinical Research Associate II in Beijing, China, to design and analyze clinical trials while ensuring compliance and data integrity. The ideal candidate should have a background in healthcare or a scientific field, along with a minimum of two years of relevant experience in clinical trial monitoring.
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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.
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: 75
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ICON Clinical Research is seeking a Clinical Research Associate II in Beijing, China, to design and analyze clinical trials while ensuring compliance and data integrity. The ideal candidate should have a background in healthcare or a scientific field, along with a minimum of two years of relevant experience in clinical trial monitoring.
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Skills & Requirements
Must-have
protocol compliance
data integrity
patient safety
site qualification
site initiation
site monitoring
site close-out visits
Nice-to-have
foster an inclusive environment
drive innovation and excellence
advancement of innovative treatments
Key Requirements
Bachelor's degree in scientific or healthcare-related 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%)