Senior / Clinical Research Associate

IQVIA UK

Good clinical practice (gcp) knowledge
International conference on harmonization (ich) guidelines
Site monitoring visit execution
The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulations

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulations.
  • Candidates will be responsible for managing subject recruitment plans and maintaining the integrity of study data.
  • The position requires evaluating site practices and escalating quality issues while ensuring proper documentation in the Trial Master File.

Matching Summary

The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulations.

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization (ICH) guidelines
  • Site monitoring visit execution
  • Subject recruitment plan tracking
  • Trial Master File (TMF) maintenance

Nice-to-have

  • Strong problem-solving skills
  • Effective time management abilities
  • Financial management experience
  • Collaborative team relationship building

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 1 year of on-site monitoring experience
  • Proficiency with Microsoft Word, Excel, and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter