Clinical Research Associate II
Clinical Careers Page(12 days ago)
About this role
ICON plc is seeking a Clinical Research Associate II to support the design and analysis of clinical trials, ensuring compliance and data quality. The role involves collaboration with site staff and investigators to facilitate study execution and contribute to clinical documentation.
Required Skills
- GCP
- Clinical Trials
- Data Review
- Regulations
- Protocol Writing
- Monitoring
- Investigator Coordination
- Data Management
- Medical Data
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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