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.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.
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
monitoring clinical trial sites
ensure adherence to study protocols
conduct site visits
data collection and reporting
training and guidance to site staff
maintain effective relationships
Nice-to-have
cross-functional team collaboration
stakeholder management skills
influence and drive compliance
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