ICON is a leading clinical research organization seeking a Senior Clinical Research Associate (CRA) in the Czech Republic to manage and monitor clinical trials, ensuring compliance with protocols and regulations. The ideal candidate will possess extensive CRA experience, strong organizational skills, and the ability to travel for site visits as needed
Job Summary
Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
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 is a leading clinical research organization seeking a Senior Clinical Research Associate (CRA) in the Czech Republic to manage and monitor clinical trials, ensuring compliance with protocols and regulations. The ideal candidate will possess extensive CRA experience, strong organizational skills, and the ability to travel for site visits as needed.
Skills & Requirements
Must-have
Clinical trial monitoring
GCP standards adherence
Site performance assessment
Data collection and reporting
Stakeholder relationship management
Nice-to-have
Fostering inclusive environment
Driving innovation and excellence
Continuous improvement focus
Key Requirements
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites and projects simultaneously
Expertise in monitoring practices, data integrity, and site management
Willingness to travel as required (approximately 60%)