Clinical Research Associate Ii / Senior Clinical Research Associate Biotech
ICON
Mechelen, Belgium
Monitoring clinical trial sites
Adherence to good clinical practice standards
Managing multiple clinical trial sites
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 focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to 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
Monitoring clinical trial sites
Adherence to Good Clinical Practice standards
Managing multiple clinical trial sites
Clinical trial data integrity
Regulatory compliance in clinical trials
Proficiency in clinical trial software
Nice-to-have
Training and guidance to site staff
Building relationships with site personnel
Multilingual communication skills
Stakeholder management skills
Problem-solving skills
Cross-functional team collaboration
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Strong understanding of clinical trial processes
Experience managing multiple sites and projects
Excellent communication in Dutch, English, and French