Clinical Site Manager II (Sr CRA)
Clinical Careers Page(2 days ago)
About this role
ICON plc is a healthcare organization focusing on clinical research. They are seeking a Senior Clinical Research Associate to oversee clinical trial activities, ensure compliance, and support trial sites to facilitate successful study executions.
Required Skills
- GCP
- Regulatory Compliance
- Site Management
- Clinical Trials Software
- Data Integrity
- Stakeholder Management
- Monitoring
- Life Sciences
- Clinical Research
Qualifications
- Advanced Degree in Life Sciences, Nursing, or Medicine
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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