Senior Clinical Research Associate
Clinical Careers Page(18 days ago)
About this role
ICON plc is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities for early phase oncology studies. The role involves ensuring compliance, data integrity, and participant safety throughout the study lifecycle, with a focus on home-based monitoring in South Korea.
Required Skills
- GCP
- Clinical Monitoring
- Site Management
- Data Integrity
- Regulatory Compliance
- Stakeholder Management
- Clinical Trial Software
- Oncology
- Monitoring Practices
- Early Phase
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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