Clinical Research Associate Ii / Senior Clinical Research Associate Large Pharma
ICON
Frankfurt, Germany
Clinical trial site monitoring
Ich-gcp guidelines knowledge
Data integrity and site management
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 focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance programme.
ICON is committed to providing an inclusive and accessible environment for all candidates and 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
ICH-GCP guidelines knowledge
Data integrity and site management
Multisite project management
German and English communication
Travel availability at least 60%
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder relationship building
Problem-solving skills
Inclusive and diverse culture
Key Requirements
Master or Bachelor's degree in scientific or healthcare field
Minimum 2 years experience as Clinical Research Associate