CRA I
Clinical Careers Page(13 days ago)
About this role
A Clinical Research Associate I at ICON plc oversees and coordinates clinical trials, ensuring compliance with regulations and managing data collection and analysis. The role involves working independently with stakeholders to support clinical study setup, monitoring, and documentation, while maintaining patient safety and regulatory adherence.
Required Skills
- GCP
- Data Review
- Study Coordination
- Regulatory Compliance
- Clinical Trials
Qualifications
- University Degree in Medicine or Science
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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