Clinical Research Associate I, II or Senior
Clinical Careers Page(18 days ago)
About this role
The role involves supporting clinical trials through site qualification, monitoring, and data review, ensuring compliance, data integrity, and patient safety. It offers the opportunity to contribute to the development of new treatments within a dynamic healthcare research environment.
Required Skills
- GCP
- Clinical Trials
- Data Review
- Regulations
- Monitoring
- Protocol
- Medical Data
- Clinical Research
- Data Integrity
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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