CRA UK - Oncology experience required
Clinical Careers Page(1 month ago)
About this role
A Senior Clinical Research Associate at ICON plc supports the conduct of oncology clinical trials within a global CRO, ensuring regulatory compliance and data quality across the study lifecycle. The UK-based role requires oncology experience and significant travel to clinical sites to support trial execution and oversight.
Required Skills
- Clinical Monitoring
- Site Management
- Data Integrity
- Good Clinical Practice
- Clinical Software
- Stakeholder Management
- Communication
- Training
- Travel
Qualifications
- Advanced Degree in Life Sciences, Nursing, or Medicine
- Valid Driver's License
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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