Clinical Site Associate

Clinical Careers Page(4 days ago)

HybridFull TimeJunior$40,000 - $55,000Clinical Operations

About this role

The Clinical Site Associate role at ICON involves supporting site management activities for clinical trials, including document collection, tracking, and coordination with stakeholders. It is based in Reading with a hybrid work setup, focusing on ensuring trial compliance and efficiency.

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Required Skills

Document Management
Clinical Trials
Data Entry
Communication
Organization

About Clinical Careers Page

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.

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