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.
You will monitor clinical trial sites, conduct site visits, collaborate with cross-functional teams, and provide training and guidance to maintain high standards of clinical trial conduct.
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
Good Clinical Practice (GCP) standards
Data integrity and site management
Cross-functional team collaboration
Travel at least 60% internationally and domestically
Nice-to-have
Training and guidance to site staff
Stakeholder relationship management
Strong organizational and problem-solving skills
Excellent communication and interpersonal skills
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive Clinical Research Associate experience
Valid driver’s license
Ability to travel at least 60% internationally and domestically