Clinical Research Associate role at ICON plc, overseeing and managing clinical trial activities, ensuring data integrity, participant safety, and compliance.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to travel at least 60% of the time
- Valid driver's license
Benefits
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits