Snr CRA
Clinical Careers Page(5 days ago)
About this role
ICON plc is seeking a Senior Clinical Research Associate to oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements. The role involves site monitoring, collaboration with teams, and supporting trial efficiency and data integrity.
Required Skills
- GCP
- Clinical Monitoring
- Data Management
- Regulatory Compliance
- Site Management
- Trial Operations
- Communication
- Problem Solving
- Travel Coordination
Qualifications
- Advanced degree in life sciences, nursing, or medicine
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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