Coordinating Cra

IQVIA UK

Not specified in the job description.
Good clinical practice gcp guidelines
International conference on harmonization ich guidelines
Site monitoring visits execution
IQVIA UK is seeking a Coordinating CRA to perform site monitoring and management across various clinical protocols. The ideal candidate should have at least five years of on-site monitoring experience and a strong understanding of GCP and ICH guidelines

Job Summary

  • The role involves performing comprehensive site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
  • Candidates will be responsible for managing study progress by tracking regulatory submissions, enrollment, data queries, and maintaining the Trial Master File.
  • This position requires acting as a mentor for clinical staff while collaborating with study teams to ensure successful project execution.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Coordinating CRA to perform site monitoring and management across various clinical protocols. The ideal candidate should have at least five years of on-site monitoring experience and a strong understanding of GCP and ICH guidelines.

Skills & Requirements

Must-have

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

Nice-to-have

  • Mentoring clinical staff members
  • Strong therapeutic protocol knowledge
  • Effective time management skills
  • Collaborative team working relationships

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 5 years of on-site monitoring experience
  • At least 1 year as a Senior CRA
  • In-depth knowledge of GCP and ICH regulations

Work Rights

Not specified

Tailored Resume

Cover Letter