CTA
Clinical Careers Page(22 days ago)
About this role
A Clinical Trial Administrator at ICON plays a key role in supporting the coordination, documentation, and regulatory compliance of clinical trials within a healthcare research setting. The position involves collaboration with cross-functional teams to ensure the smooth execution of clinical studies and contribute to the development of innovative medical treatments.
Required Skills
- Clinical Trials
- Regulatory Compliance
- Documentation
- Medical Data Analysis
- Study Coordination
- Informed Consent
- Case Report Forms
- Data Tracking
- Healthcare
Qualifications
- Bachelor's degree in a scientific or healthcare-related field
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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