As a 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 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.
You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
ICON plc is a world-leading healthcare intelligence and clinical research organization, proud to foster an inclusive environment driving innovation and excellence.
Matching Summary
As a 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
Oversee clinical trial activities
Ensure data integrity and participant safety
Monitor clinical trial sites
Conduct site visits and provide support
Collaborate with cross-functional teams
Build effective relationships with stakeholders
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Shape the future of clinical development
Nurture talent and reward high performance
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Experience as a Clinical Research Associate
Strong understanding of clinical trial processes
Proven ability to manage multiple sites and projects