ICON plc is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities, ensuring compliance with protocols and regulatory standards. The ideal candidate will possess extensive CRA experience, an advanced degree in a relevant field, and strong organizational and communication skills. The position offers competitive compensation and a range of benefits, fostering a diverse and inclusive work environment
Job Summary
As a Senior 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.
In addition to your competitive salary, 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 plc is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities, ensuring compliance with protocols and regulatory standards. The ideal candidate will possess extensive CRA experience, an advanced degree in a relevant field, and strong organizational and communication skills. The position offers competitive compensation and a range of benefits, fostering a diverse and inclusive work environment.
Skills & Requirements
Must-have
Adherence to study protocols
Regulatory requirements and GCP standards
Site performance assessment
Timely data collection and reporting
Training site staff and CRAs
Building effective relationships
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Shaping the future of clinical development
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites and projects