Sr. Clinical research Associate
Clinical Careers Page(3 days ago)
About this role
A Senior Clinical Research Associate at ICON plc oversees clinical trial activities, ensuring compliance with protocols and regulatory standards. The role involves site monitoring, data integrity assurance, and collaboration with cross-functional teams to support successful completion of clinical studies.
Required Skills
- GCP
- Clinical Monitoring
- Site Management
- Data Integrity
- Regulatory Compliance
- Clinical Trials Software
- Communication
- Stakeholder Management
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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