Clinical Research Associate Ii/ Senior Clinical Research Associate
ICON
Hong Kong, Hong Kong
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and compliance
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Job Summary
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
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.
At ICON, inclusion & belonging are fundamental to our culture and values, and the company is dedicated to providing an inclusive and accessible environment for all candidates.
Matching Summary
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Skills & Requirements
Must-have
Clinical trial site monitoring
Good Clinical Practice (GCP) standards
Data integrity and compliance
Site management and performance assessment
Cross-functional team collaboration
International and domestic travel up to 60%
Nice-to-have
Training and guidance to site staff
Stakeholder relationship management
Problem-solving and organizational skills
Inclusive and diverse work culture
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive Clinical Research Associate experience
Valid driver’s license
Ability to travel at least 60% internationally and domestically