ICON is seeking a Clinical Research Associate II based in Changchun, China. The role involves conducting clinical trial monitoring activities and ensuring compliance with protocols while fostering a collaborative environment
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 designed to be competitive within each country and focused on well-being and work life balance opportunities.
Matching Summary
Match Score: 85
ICON is seeking a Clinical Research Associate II based in Changchun, China. The role involves conducting clinical trial monitoring activities and ensuring compliance with protocols while fostering a collaborative environment.
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
collaborative work environment
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%)