UK Clinical Research Associate – On-Site Monitoring

UK Clinical Research Associate – On-Site Monitoring

Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
IQVIA

At a Glance

  • Tasks: Monitor clinical sites and ensure compliance with study protocols and regulations.
  • Company: Join IQVIA, a leader in clinical research with a focus on innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Dynamic role with opportunities for site visits and collaboration with diverse teams.
  • Why this job: Make a difference in healthcare by ensuring studies run smoothly and effectively.
  • Qualifications: Experience in clinical research and strong organisational skills.

The predicted salary is between 40000 - 50000 Β£ per year.

IQVIA c FSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

Perform monitoring and site management to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Responsibilities include site visits, monitoring, recruitment tracking, protocol training, regulatory compliance, TMF/ISF documentation, and collaboration with study teams.

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UK Clinical Research Associate – On-Site Monitoring employer: IQVIA

IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.

IQVIA

Contact Details:

IQVIA Recruitment Team

We think you need these skills to ace UK Clinical Research Associate – On-Site Monitoring

Site Monitoring
Site Management
Study Protocol Compliance
Regulatory Compliance
TMF/ISF Documentation
Recruitment Tracking
Protocol Training