Clinical Research Associate
ICON · Reading, UK
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Clinical Research Associate II in Reading to monitor clinical trials, ensure protocol compliance, and maintain data integrity. The role involves site visits, investigator collaboration, and documentation review within a sponsor-dedicated model.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years clinical research associate experience
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Willingness to travel approximately 60% as required
- Legal right to work in the UK
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff to facilitate study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation and reports
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.