Senior Clinical Research Associate - UK (60% Travel) in Reading

Senior Clinical Research Associate - UK (60% Travel) in Reading

Reading Full-Time 37800 - 46200 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Monitor clinical trials and ensure compliance with protocols and regulations.
  • Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
  • Benefits: Competitive salary, travel opportunities, and professional development.
  • Other info: Dynamic role with opportunities for growth in a fast-paced environment.
  • Why this job: Make a real difference in healthcare while travelling and collaborating with diverse teams.
  • Qualifications: Strong CRA experience and willingness to travel up to 60%.

The predicted salary is between 37800 - 46200 Β£ per year.

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior CRA in the UK.

The role focuses on monitoring clinical trials and ensuring adherence to protocol, regulatory standards, and GCP.

You will conduct site visits, support trial execution, and collaborate with cross-functional teams to ensure timely data collection and reporting.

Strong CRA experience and travel up to 60% are required.

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Senior Clinical Research Associate - UK (60% Travel) in Reading employer: ICON

At ICON plc, we pride ourselves on being an exceptional employer that values innovation and collaboration in the healthcare intelligence and clinical research sector. Our supportive work culture fosters professional growth through continuous learning opportunities and a commitment to diversity, ensuring that every employee can thrive while making a meaningful impact in the industry. Located in a dynamic environment, we offer unique advantages such as access to cutting-edge resources and a network of talented professionals dedicated to excellence.

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Contact Details:

ICON Recruitment Team

We think you need these skills to ace Senior Clinical Research Associate - UK (60% Travel) in Reading

Clinical Trial Monitoring
Regulatory Standards Knowledge
Good Clinical Practice (GCP)
Site Visit Coordination
Data Collection and Reporting
Cross-Functional Team Collaboration
Strong CRA Experience