Clinical Research Associate Ii / Senior Clinical Research Associate Biotech
ICON
Frankfurt, Germany
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and 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.
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 and belonging are fundamental to the culture and values, and the company is dedicated to providing an inclusive and accessible environment for all candidates.
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 compliance
Site management and performance assessment
Proficiency in clinical trial software
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder relationship management
Bilingual communication in German and English
Problem-solving and organizational skills
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive Clinical Research Associate experience
Strong understanding of clinical trial processes
Excellent communication skills in German and English