ICON Clinical Research is seeking a Senior Clinical Research Associate (CRA) to manage clinical trial activities in the Czech Republic. The ideal candidate will have extensive experience in clinical trial monitoring and a strong understanding of regulatory requirements, along with excellent communication skills
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 Clinical Research is seeking a Senior Clinical Research Associate (CRA) to manage clinical trial activities in the Czech Republic. The ideal candidate will have extensive experience in clinical trial monitoring and a strong understanding of regulatory requirements, along with excellent communication skills.
Skills & Requirements
Must-have
clinical trial monitoring
protocol adherence
regulatory requirements
GCP standards
site performance assessment
data integrity
stakeholder management
Nice-to-have
foster an inclusive environment
drive innovation and excellence
nurtures talent
well-being and work life balance
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
Willingness to travel as required (approximately 60%)