Clinical Research Associate II - Flexible Work & AI Tools in London

Clinical Research Associate II - Flexible Work & AI Tools in London

London Full-Time 40000 - 48822 Β£ / year (est.) Home office (partial)
IQVIA LLC

At a Glance

  • Tasks: Conduct site monitoring visits and ensure compliance with guidelines.
  • Company: Join IQVIA, a leader in healthcare innovation.
  • Benefits: Flexible work options and opportunities for career advancement.
  • Other info: Be part of a team dedicated to enhancing healthcare integrity.
  • Why this job: Make a difference in healthcare while using cutting-edge AI tools.
  • Qualifications: 12 months of monitoring experience and a degree in a scientific field.

The predicted salary is between 40000 - 48822 Β£ per year.

IQVIA LLC is seeking a Clinical Research Associate II to perform site monitoring visits in South East England. The role encompasses responsibilities including adherence to GCP and ICH guidelines, recruitment tracking, and ensuring protocol compliance.

Candidates should have at least 12 months of monitoring experience and a degree in a scientific discipline. This full-time position offers opportunities for career growth and flexible working arrangements.

Join IQVIA in enhancing healthcare through innovative solutions while contributing to the integrity of the hiring process.

Clinical Research Associate II - Flexible Work & AI Tools in London employer: IQVIA LLC

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. Our commitment to employee growth is evident through our flexible working arrangements and the use of cutting-edge AI tools, empowering our Clinical Research Associates to excel in their roles while making a meaningful impact in healthcare across South East England.

IQVIA LLC

Contact Details:

IQVIA LLC Recruitment Team

We think you need these skills to ace Clinical Research Associate II - Flexible Work & AI Tools in London

GCP (Good Clinical Practice)
ICH (International Council for Harmonisation) Guidelines
Site Monitoring
Recruitment Tracking
Protocol Compliance
Monitoring Experience
Scientific Discipline Degree