Clinical Research Associate II - Global Trial Monitoring in Belfast

Clinical Research Associate II - Global Trial Monitoring in Belfast

Belfast Full-Time 40500 - 49500 £ / year (est.) No working from home possible
ICON

At a Glance

  • Tasks: Design and analyse clinical trials while ensuring patient safety and data integrity.
  • Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
  • Benefits: Competitive salary, travel opportunities, and professional development in a dynamic field.
  • Other info: Exciting opportunity for career growth in a global organisation.
  • Why this job: Make a real difference in innovative therapies and contribute to healthcare advancements.
  • Qualifications: Experience in clinical research and strong analytical skills required.

The predicted salary is between 40500 - 49500 £ per year.

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re looking for a Clinical Research Associate II/III to design and analyse trials, interpret complex medical data, and contribute to advances in innovative therapies.

As CRA you will:

  • Conduct site qualification, initiation, monitoring and close-out visits
  • Ensure protocol compliance, data integrity and patient safety
  • Collaborate with investigators and site staff to support study conduct

Travel approx.

Clinical Research Associate II - Global Trial Monitoring in Belfast employer: ICON

ICON plc is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the healthcare intelligence and clinical research sector. With a strong commitment to employee growth, you will have access to mentorship opportunities and the chance to lead diverse teams, all while enjoying the flexibility of travel and a supportive environment that values your contributions.

ICON

Contact Details:

ICON Recruitment Team

We think you need these skills to ace Clinical Research Associate II - Global Trial Monitoring in Belfast

Clinical Trial Design
Data Analysis
Medical Data Interpretation
Site Qualification
Monitoring Visits
Protocol Compliance
Data Integrity