Site qualification, initiation, monitoring, and close-out visits
ICON plc is seeking a Clinical Research Associate II (CRA II) in Santiago, Chile, to contribute to clinical trial monitoring activities. The ideal candidate should have a background in healthcare or scientific fields, with at least two years of relevant experience
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.
Matching Summary
Match Score: 85
ICON plc is seeking a Clinical Research Associate II (CRA II) in Santiago, Chile, to contribute to clinical trial monitoring activities. The ideal candidate should have a background in healthcare or scientific fields, with at least two years of relevant experience.
Skills & Requirements
Must-have
Clinical trial monitoring activities
Protocol compliance and patient safety
Site qualification, initiation, monitoring, and close-out visits
Data review and query resolution
ICH-GCP guidelines knowledge
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Contributing to advancement of treatments
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years of experience as a Clinical Research Associate