At a Glance
- Tasks: Monitor clinical trials, ensure compliance, and collaborate with diverse teams.
- Company: Leading healthcare intelligence and clinical research organisation committed to excellence.
- Benefits: Competitive salary, travel opportunities, and a focus on inclusion.
- Other info: Dynamic role with opportunities for professional growth in a supportive environment.
- Why this job: Shape the future of clinical development while making a real impact.
- Qualifications: 18+ months CRA experience and willingness to travel 60%.
The predicted salary is between 36900 - 45100 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re committed to inclusion and excellence as we shape the future of clinical development.
The Clinical Research Associate (CRA) role focuses on monitoring trial activities, ensuring protocol compliance, data integrity, and collaboration across cross-functional teams.
The position requires 18+ months CRA experience, near to 4 years for SCRA level, and willingness to travel about 60%.
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Senior Clinical Research Associate — UK Travel & Site Monitoring in Reading employer: ICON Strategic Solutions
ICON plc is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for EDC Trial Design Specialists to thrive. With a strong emphasis on employee growth and development, you will have access to continuous training and career advancement opportunities, all while working in a dynamic environment that values quality and compliance in clinical trials.
