Site qualification, initiation, monitoring, close-out
Protocol compliance, data integrity, patient safety
Collaboration with investigators and site staff
ICON Clinical Research is seeking a Clinical Research Associate II in Nanjing, China. Ideal candidates will have a background in clinical research, particularly with a focus on trial processes and regulations, and will thrive in a collaborative, fast-paced environment
Job Summary
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
Matching Summary
Match Score: 85
ICON Clinical Research is seeking a Clinical Research Associate II in Nanjing, China. Ideal candidates will have a background in clinical research, particularly with a focus on trial processes and regulations, and will thrive in a collaborative, fast-paced environment.
Skills & Requirements
Must-have
Site qualification, initiation, monitoring, close-out
Protocol compliance, data integrity, patient safety
Collaboration with investigators and site staff
Data review and query resolution
Study documentation preparation and review
Nice-to-have
Fostering inclusive environment
Driving innovation and excellence
Advancing innovative treatments and therapies
Nurturing talent
Work-life balance opportunities
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, ICH-GCP