Clinical Research Associate
Clinical Careers Page(14 days ago)
About this role
This role involves supporting the design, analysis, and conduct of clinical trials, ensuring compliance and data integrity. The position requires collaborating with investigators and site staff to facilitate study implementation and contribute to clinical documentation.
Required Skills
- GCP
- Clinical Trials
- Data Review
- Regulations
- Monitoring
Qualifications
- Bachelor's Degree in a scientific or healthcare-related field
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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