Clinical Study Administrator (CTA level)
Clinical Careers Page(27 days ago)
About this role
ICON plc is a renowned clinical research organization dedicated to advancing healthcare through innovative clinical development. The role involves supporting clinical trial documentation, submission preparation, and administrative oversight to ensure study compliance and readiness.
Required Skills
- Veeva
- eTMF
- Clinical Trials
- Regulatory Submissions
- Document Management
- GCP
- Start-up Procedures
- Vendor Management
- Organizational Skills
- Communication
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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