CRA I
Clinical Careers Page(1 day ago)
About this role
ICON plc is a global healthcare organization specializing in clinical research. They are currently seeking a Clinical Research Associate I to support Phase II–IV clinical trials in France, focusing on site monitoring and regulatory compliance.
Required Skills
- GCP
- Clinical Trials
- Site Monitoring
- Source Data Verification
- Regulatory Compliance
- Data Management
- French
- English
- Pharmacovigilance
- Study 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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