Senior CTA
Clinical Careers Page(12 days ago)
About this role
ICON plc is seeking a Senior Clinical Trial Assistant to support clinical research operations by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice guidelines. The role involves coordinating site activities, assisting with regulatory documents, and fostering effective communication with trial sites.
Required Skills
- GCP
- Clinical Trial
- Site Management
- Regulatory Documents
- Data Analysis
- Monitoring
- Communication
- Project Management
- Experience in Clinical Research
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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