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As a Study Support Assistant at ICON, you will provide administrative and operational support for clinical trials, contributing to the advancement of innovative treatments and therapies.
Job Responsibility
Assisting with the preparation and distribution of study documents, including protocols, informed consent forms, and regulatory submissions
Coordinating study-related meetings and maintaining meeting minutes and action items
Managing study-related correspondence, including emails, phone calls, and faxes
Supporting study teams in the maintenance of study files and documentation, ensuring compliance with regulatory requirements and company procedures
Assisting with the tracking and management of study-related materials and supplies
Requirements
High school diploma or equivalent required
Bachelor's degree preferred
Previous administrative or clerical experience, preferably in a healthcare or clinical research setting
Strong organizational skills and attention to detail
Excellent communication and interpersonal skills, with the ability to work effectively in a team environment
Proficiency in Microsoft Office suite (Word, Excel, Outlook)
What we offer
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others