ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
About the role
We are currently seeking a Site Specialist II to join our diverse and dynamic team. As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contributing to efficient study start-up and maintenance.
What You Will Be Doing:
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Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies.
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Acting as an operational liaison for site staff on documentation, systems, and process-related questions.
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Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools.
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Supporting planning and logistics for site meetings, investigator meetings, and monitoring visits.
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Identifying opportunities to streamline site workflows and contributing to process improvement initiatives.
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Providing guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development.