Clinical Registry Coordinator
Clinical Careers Page(2 months ago)
About this role
Clinical Registry Coordinator at ICON supporting a large pharmaceutical client within the clinical development function. The position is based in the clinical registry group of a CRO and interfaces with global, cross-functional teams and external partners. It is positioned to support clinical trial registry governance and disclosure alignment across regions.
Required Skills
- Clinical Registry
- Clinical Research
- Document Management
- Project Management
- Vendor Management
- Data Analysis
- Microsoft Office
- Cross Functional
- Written Communication
Qualifications
- Bachelor's Degree in Health or Science
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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