Clinical Study Administrator (CTA level)
Clinical Careers Page(1 month ago)
About this role
A Clinical Trial Associate (Clinical Study Administrator) at ICON supports clinical research studies by overseeing study documentation, regulatory recordkeeping, and local study administration. The role acts as a local contact for study teams and contributes to maintaining inspection-ready trial records while collaborating with cross-functional and external partners.
Required Skills
- Document Management
- eTMF
- Veeva
- Vendor Management
- Regulatory Submissions
- Clinical Trials
- ICH-GCP
- Communication
- Organization
- Time Management
Qualifications
- BS/BA Degree
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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