Clinical Site Associate

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Clinical Site Associate/ Inhouse CRA/ Milan, Italy
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.
As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.
What You Will Do You will contribute to scientific operations activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities Include Supporting site activation activities, including the collection,



review, and tracking of essential documents and approvals.
Maintaining up-to-date site information and status in clinical trial management systems and trackers.
Assisting CRAs and project teams with site communications, follow-up, and resolution of site-level queries.
Coordinating logistics for site visits and meetings, including scheduling, documentation preparation, and follow-up actions.
Ensuring accurate filing and maintenance of essential documents to support inspection and audit readiness.
Collaborating with internal stakeholders to support timely site

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8cifla