Site Specialist II
Clinical Careers Page(3 days ago)
About this role
The Site Specialist II at ICON manages site support activities, coordinating documentation, assisting with study start-up and maintenance, and supporting process improvements within clinical trials. The role involves interaction with site staff, ensuring compliance, and maintaining project metrics to facilitate the clinical research process.
Required Skills
- GCP
- Clinical Trials
- Documentation
- Site Coordination
- Project Management
- Communication
- Problem Solving
- Process Improvement
About Clinical Careers Page
iconplc.comICON 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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