CRA2
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate II at ICON supports clinical development by working on clinical trials, contributing to study design and data interpretation, and helping advance innovative treatments. The role is part of ICON’s global clinical research organization and is based home‑based from Wuhan with substantial travel to study sites.
Required Skills
- Site Monitoring
- Protocol Compliance
- Data Review
- Query Resolution
- ICH-GCP
- Study Documentation
- Communication
- Organization
- Patient Safety
- Travel
Qualifications
- Bachelor's Degree
- Driver's License
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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