Clinical Research Associate 3
Clinical Careers Page(2 months ago)
About this role
A Senior Clinical Research Associate at ICON plc oversees and supports the conduct of clinical trials to ensure participant safety, data integrity, and regulatory compliance. The role involves working across study sites and teams to support trial execution and maintain high standards in clinical development.
Required Skills
- Monitoring
- Site Visits
- Site Management
- Data Integrity
- Protocol Compliance
- GCP
- Clinical Software
- Stakeholder Management
- Project Management
Qualifications
- Advanced Degree (Life Sciences/Nursing/Medicine)
- Valid Driver's License
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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