Clinical Research Coordinator - London

IQVIA UK

London, United Kingdom
Clinical trial coordination
Patient data collection
Study documentation management
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries

Job Summary

  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
  • This is a short-term study assignment (1–2 months), working 30–40 hours per week, supporting two sites in Central London conducting a pediatric clinical trial in ophthalmology.
  • As a pivotal member of the site team, you will be involved in a variety of clinical and administrative tasks to support investigators, ensure the smooth running of clinical trials, and assist with the collection of patient data.

Matching Summary

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Skills & Requirements

Must-have

  • Clinical trial coordination
  • Patient data collection
  • Study documentation management
  • Protocol compliance
  • Clinical study set-up
  • Strong IT skills
  • Participant recruitment and screening

Nice-to-have

  • Pediatric clinical trial experience
  • Ophthalmology clinical trial experience
  • Excellent interpersonal skills
  • Strong organizational skills
  • Ability to build effective working relationships

Key Requirements

  • BS/BA in life sciences or equivalent
  • Relevant clinical or medical work experience
  • Experience as Research Nurse or Clinical Research Coordinator
  • Knowledge of clinical trial procedures
  • Proficiency in Microsoft Office applications

Work Rights

Not specified

Tailored Resume

Cover Letter