Clinical Research Associate
ICON · Reading, UK
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks an experienced Clinical Research Associate II to design and analyze clinical trials, monitor study sites, and ensure protocol compliance in a sponsor-dedicated model. The role involves regional travel throughout the Midlands and requires 2+ years of CRA experience with strong regulatory knowledge.
What they're looking for
- Bachelor's degree in science or healthcare field
- Minimum 2 years of Clinical Research Associate experience
- In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulations
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environments
- Willingness to travel approximately 60% as required
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial conduct
- Collaborate with investigators and site staff to facilitate smooth study operations
- Perform data review and query resolution to maintain high-quality clinical data
- Contribute to preparation and review of study documentation and clinical study 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.