Clinical Resaerch Associate - Sponsor Dedicated - Cardiovascular Area
ICON
Clinical trial site monitoring
Adherence to study protocols
Gcp standards compliance
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
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.
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 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
Clinical trial site monitoring
Adherence to study protocols
GCP standards compliance
Data integrity and participant safety
Site performance assessment
Effective stakeholder relationships
Nice-to-have
Fostering inclusive environment
Driving innovation and excellence
Shaping future of clinical development
Work life balance opportunities
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate