Clinical Research Associate I
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate I at ICON plc supports the coordination and monitoring of clinical trials within a global healthcare intelligence and clinical research organization. The role focuses on ensuring regulatory compliance, accurate data collection, and collaboration with investigators and site staff.
Required Skills
- Clinical Monitoring
- Regulatory Compliance
- ICH-GCP Knowledge
- Data Collection
- Study Documentation
- Stakeholder Management
- Patient Safety
- Communication
- Travel
Qualifications
- University Degree in Medicine or Science
- Valid Driver's License
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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