As a Senior CRA at ICON Plc, you will oversee and manage 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 oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
You will 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 opportunities for you and your family.
Matching Summary
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Skills & Requirements
Must-have
Clinical trial monitoring tasks
Adherence to study protocols
Regulatory requirements and GCP
Conducting site visits
Cross-functional team collaboration
Site staff training and guidance
Relationship building with stakeholders
Nice-to-have
Fostering an 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
Proficiency in relevant clinical trial software and tools
Willingness to travel as required (approximately 60%)