Clinical Research Associate (Start Up) - Oncology - Illinois
Clinical Careers Page(7 days ago)
About this role
A Clinical Research Associate at ICON specializes in managing the startup phase of oncology clinical trials. The role involves site qualification, site activation, and ensuring regulatory compliance, all while maintaining strong relationships with clinical sites and managing documentation.
Required Skills
- GCP
- ICH Guidelines
- Regulatory Affairs
- Site Qualification
- Trial Management
- Clinical Monitoring
- CTMS
- EDC
- Trial Documentation
- Oncology
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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