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
Good Clinical Practice (GCP) standards
Site performance assessment
Data integrity and site management
Relevant clinical trial software and tools
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Shape the future of clinical development
Nurture talent and reward high performance
Focus on well-being and work-life balance
Key Requirements
Bachelor's degree in relevant scientific or healthcare field
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites and projects
Strong organizational and problem-solving skills
Excellent communication, interpersonal, and stakeholder management skills