Clinical Research Associate
Clinical Careers Page(2 months ago)
About this role
A Clinical Research Associate I at ICON plc supports the design and execution of clinical trials within a global healthcare intelligence and clinical research organization. The role contributes to advancing treatments by ensuring high-quality clinical data and adherence to regulatory standards. The position works closely with study teams and external investigators to support study conduct and reporting.
Required Skills
- Monitoring
- Protocol Compliance
- Data Review
- Patient Safety
- Study Documentation
- Query Resolution
- ICH-GCP
- Communication
- Organization
- Travel
Qualifications
- Bachelor's Degree in Scientific or Healthcare Field
- 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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