Clinical Site Associate
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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
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Clinical Site Associate
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Milan, Lombardy, Italia ICON San Antonio Tempo pienoICON is seeking a Clinical Site Associate in Milan to support site management activities and ensure trials are conducted efficiently and in compliance.Si candidi (facendo clic sul pulsante apposito) dopo aver controllato tutte le informazioni di lavoro riportate di seguito.You will contribute to operations, collaborate with CRAs, and help maintain trial...
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Milan, Lombardy, Italia ICON San Antonio Tempo pienoICON is seeking a Clinical Site Associate in Milan to support site management activities and ensure trials are conducted efficiently and in compliance. You will contribute to operations, collaborate with CRAs, and help maintain trial documentation and systems.The role requires a life sciences background, experience in clinical research or regulated...
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