Clinical Research Associate
Clinical Careers Page(3 days ago)
About this role
A Clinical Research Associate at ICON plays a key role in managing and monitoring clinical trials, ensuring compliance, data integrity, and patient safety. The role involves collaboration with investigators and site staff to facilitate study conduct and documentation review.
Required Skills
- clinical Monitoring
- ICH-GCP
- Data Review
- Regulatory Compliance
- Medical Data Analysis
- Clinical Trials
- Site Management
- Protocol Review
- Medical Data Interpretation
- Patient Safety
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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