About this role
ICON plc is a leading healthcare organization specializing in clinical research. The company fosters an inclusive environment, emphasizing innovation, excellence, and a commitment to improving patients' lives through clinical development. The role involves working within a dynamic team to support clinical trials in a fast-paced setting.
Required Skills
- GCP
- Clinical Trials
- Monitoring
- Regulatory Submissions
- Medical Data Evaluation
- Study Start-up
- Study Close-out
- Documentation
- Communication
- Travel
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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