CRAII / Senior CRA
Clinical Careers Page(8 days ago)
About this role
A Clinical Research Associate at ICON is responsible for overseeing various phases of clinical trials to ensure protocol compliance, data quality, and patient safety. The role involves collaboration with investigators and site staff, performing site visits, and reviewing study documentation to support clinical development efforts in a global biotechnology organization.
Required Skills
- clinical Trials
- GCP
- Regulations
- Data Review
- Site Monitoring
Qualifications
- Bachelor's Degree in a 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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