Senior CRA
Clinical Careers Page(2 days ago)
About this role
ICON plc is seeking a Senior Clinical Research Associate to oversee clinical trial activities, ensuring compliance with protocols, regulations, and industry standards. The role supports the successful execution of trials by monitoring sites, managing data integrity, and maintaining stakeholder relationships.
Required Skills
- GCP
- Monitoring
- Data Management
- Site Management
- Clinical Trials
- Regulatory Compliance
- Data Integrity
- Communication
- Stakeholder Management
- Travel Coordination
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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