Clinical Research Associate
Clinical Careers Page(12 days ago)
About this role
ICON plc is seeking experienced Clinical Research Associates to oversee and manage clinical trial activities, ensuring compliance with protocols and regulatory standards. The role involves site monitoring, coordination with teams, and maintaining data integrity in Romania. It offers opportunities for professional growth in a global healthcare organization.
Required Skills
- Clinical Monitoring
- GCP
- Site Management
- Data Integrity
- Regulatory Compliance
- Good Clinical Practice
- Trial Coordination
- Communication
- Stakeholder Management
- Clinical Trials Software
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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