Clinical Research Associate II
Clinical Careers Page(18 days ago)
About this role
A Clinical Research Associate at ICON plays a key role in managing and monitoring clinical trials to ensure compliance, data integrity, and patient safety. The position involves collaboration with study teams, site management, and documentation review, supporting innovative medical treatments and therapies.
Required Skills
- clinical Trials
- Data Review
- GCP Guidelines
- Regulatory Compliance
- Site Management
- Medical Data
- Documentation
- Monitoring
- Communication
- Organization
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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