Clinical Research Associate (cra) - Ofthalmology Area
ICON
Frankfurt, Germany
Clinical trial site monitoring
Good clinical practice (gcp) standards
Ophthalmology clinical research experience
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.
ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
At ICON, inclusion & belonging are fundamental to our culture and values, and the company is committed to providing a workplace free of discrimination and harassment.
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
Ophthalmology clinical research experience
Fluency in English and German
Ability to travel internationally and domestically
Valid driver’s license
Nice-to-have
Cross-functional team collaboration
Training and guidance to site staff
Stakeholder management skills
Problem-solving and organizational skills
Inclusive and diverse work culture
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate