CRA II/Sr CRA - Sponsor Dedicated
ICON · North London (accellacare), UK +5 more
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Clinical Research Associate II or Senior CRA for sponsor-dedicated clinical trial monitoring across UK locations. The role involves overseeing trial sites, ensuring regulatory compliance, managing data integrity, and guiding site staff within a global contract research organization.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with strong regulatory knowledge
- Ability to manage multiple sites and projects with organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software
- Strong communication and stakeholder management abilities
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on accurate data collection and reporting
- Train site staff and other CRAs on clinical trial conduct standards
- Build and maintain effective relationships with site personnel and trial stakeholders
Privacy & handoff
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