Senior Clinical Research Associate (SCRA) - sponsor dedicated
Clinical Careers Page(3 months ago)
About this role
A Senior Clinical Research Associate at ICON plc is responsible for overseeing and managing clinical trial activities across study sites to ensure protocol adherence, regulatory compliance, and participant safety. The role supports data integrity and contributes to successful trial execution within a global clinical research organization.
Required Skills
- Monitoring
- Site Visits
- Data Integrity
- Regulatory Compliance
- GCP
- Site Management
- Training
- Stakeholder Management
- Communication
- Clinical Software
+3 more
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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