Clinical Research Associate
ICON · Reading, UK
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks Clinical Research Associates for its oncology partnership in the UK South-West region. The role involves monitoring trial sites, ensuring protocol compliance and data quality, and supporting study delivery across multiple locations.
What they're looking for
- Degree in Life Sciences, Nursing, Medicine, or related discipline
- Previous UK experience as Clinical Research Associate in oncology studies
- Strong understanding of clinical trial processes, regulatory requirements, and GCP
- Proven site management and monitoring experience
- Excellent organisational skills managing multiple sites and priorities
- Strong communication and relationship-building abilities
- Valid UK driving licence and willingness to travel across South-West region
What you'll be doing
- Monitor clinical trial sites for protocol compliance, ICH-GCP adherence, and regulatory requirements
- Conduct on-site visits across South-West UK to support sites and resolve operational challenges
- Collaborate with cross-functional teams on accurate and timely data collection and reporting
- Build and maintain relationships with investigators, site staff, and key stakeholders
- Guide site personnel on successful clinical trial delivery
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.