Senior CRA
Clinical Careers Page(26 days ago)
About this role
A Senior Clinical Research Associate at ICON plc is responsible for overseeing clinical trial activities to support study execution and ensure adherence to protocols, regulations, and industry standards. The role focuses on maintaining data integrity and participant safety across the study lifecycle while representing ICON with trial sites and stakeholders. It contributes to successful trial outcomes through clinical oversight and collaboration with cross-functional teams.
Required Skills
- Monitoring
- Site Management
- Data Integrity
- GCP
- Protocol Compliance
- Clinical Software
- Stakeholder Management
- Communication
- Training
- Project Management
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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