About this role
Role Overview
- Drive study performance at the sites
- Perform site monitoring and other onsite visit activities
- Provide the required monitoring visit reports within required timelines
- Proactively identify study-related issues and escalates to Local Study Teams
- Train, support and advise Investigators and site staff in study related matters
Requirements
- Minimum 2-year experience as CRA
- Understanding of the clinical dataflow
- Good knowledge of the clinical study and drug development processes
- Fluent in both oral and written English
- Bachelor's degree in biological science or healthcare-related field, or equivalent
Benefits
- Health insurance
- Professional development opportunities
- Flexible working arrangements