This role focuses on administrative support and includes a structured, alternating weekly on-site schedule across Liverpool and Campbelltown
Job Summary
This role focuses on administrative support and includes a structured, alternating weekly on-site schedule across Liverpool and Campbelltown.
Your Responsibilities include general clinical trial administrative support, preparing and organising study documentation, assisting with site file maintenance, supporting recruitment activities, scheduling support for study visits, and liaising with site staff and stakeholders.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
This role focuses on administrative support and includes a structured, alternating weekly on-site schedule across Liverpool and Campbelltown.
Skills & Requirements
Must-have
Clinical trial administrative support
Study documentation preparation
Site file maintenance
Recruitment activity assistance
Scheduling study visits
Liaising with site staff
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Nurturing talent
Focus on well-being and work life balance
Key Requirements
Previous experience in clinical research
Clinical research site administration experience
Strong organisational skills
Attention to detail
Ability to work independently across multiple locations