Sr. Clinical Research Associate
Clinical Careers Page(11 days ago)
About this role
ICON plc is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring compliance with protocols, regulatory standards, and industry best practices. The role focuses on site monitoring, data integrity, and participant safety, contributing to successful clinical trial execution.
Required Skills
- GCP
- Clinical Trial
- Site Management
- Monitoring
- Data Integrity
- Regulatory Compliance
- Communication
- Problem Solving
- Travel Management
- Clinical Software
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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