Cra 2 - Single Sponsor Dedicated

IQVIA UK

United Kingdom
Site monitoring visits
Subject recruitment plan
Protocol and study training
Join IQVIA cFSP (sponsor-dedicated) as an experienced Clinical Research Associate in the UK to drive healthcare forward

Job Summary

  • Join IQVIA cFSP (sponsor-dedicated) as an experienced Clinical Research Associate in the UK to drive healthcare forward.
  • Perform essential functions including site monitoring, recruitment planning, training, quality evaluation, and documentation management.
  • This role requires a Bachelor's Degree in a scientific or healthcare discipline and at least 1 year of on-site monitoring experience.

Matching Summary

Join IQVIA cFSP (sponsor-dedicated) as an experienced Clinical Research Associate in the UK to drive healthcare forward.

Skills & Requirements

Must-have

  • Site monitoring visits
  • Subject recruitment plan
  • Protocol and study training
  • Quality and integrity evaluation
  • Trial Master File maintenance
  • Site management documentation

Nice-to-have

  • Collaboration with study team
  • Effective time management
  • Problem-solving skills

Key Requirements

  • 1 year on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good Clinical Practice (GCP) knowledge
  • ICH guidelines knowledge
  • Proficiency in Microsoft Office Suite
  • Written and verbal communication skills in English

Work Rights

Not specified

Tailored Resume

Cover Letter