As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. The role involves leading on clinical trial monitoring tasks, conducting site visits, collaborating with cross-functional teams, and building effective relationships with site personnel and stakeholders.
Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- 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
Benefits
- Various annual leave entitlements
- Health insurance
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
