CRA 2
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate II at ICON contributes to the execution and oversight of clinical trials, supporting the integrity of trial data and the advancement of new treatments. The role sits within ICON’s clinical research organization and involves collaboration with investigators and study teams to support clinical development.
Required Skills
- Site Monitoring
- Site Initiation
- Site Close-Out
- Protocol Compliance
- Data Review
- Query Resolution
- ICH-GCP
- Patient Safety
- Study Documentation
- Communication
Qualifications
- Bachelor's Degree
- 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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