CRAI
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate at ICON plc supports the conduct of clinical trials by overseeing study setup, monitoring, and documentation to ensure compliance with regulatory and company standards. The role contributes to clinical development by maintaining data integrity, supporting patient safety, and collaborating with investigators and site staff across international studies.
Required Skills
- Clinical Monitoring
- Study Coordination
- Regulatory Compliance
- Data Analysis
- Medical Review
- Communication
- Stakeholder Management
- Travel
Qualifications
- University Degree (Medicine or Science)
- Valid Driver's License
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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