(senior) Clinical Research Associate - Sponsor Dedicated
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 additional 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
Data integrity and compliance
Multisite project management
Proficiency in clinical trial software
Fluency in German and English
Valid driver’s license and travel ability
Nice-to-have
Strong organizational skills
Stakeholder management
Cross-functional team collaboration
Training and guidance provision
Problem-solving skills
Inclusive and diverse culture
Key Requirements
Advanced degree in life sciences, nursing, or medicine