Clinical Research Associate (cra) - Ofthalmology Area
ICON plc
Switzerland
Monitoring clinical trial sites
Conducting site visits
Collaborating with cross-functional teams
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.
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
Conducting site visits
Collaborating with cross-functional teams
Providing training and guidance
Building and maintaining relationships
Ophthalmology experience required
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Nurturing talent
Focus on well-being and work life balance
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