Sr. Cra 1 - Single Sponsor Dedicated

IQVIA

UK
Not specified
Good clinical practice (gcp) knowledge
Site monitoring visit execution
Subject recruitment plan management
IQVIA is seeking experienced Senior Clinical Research Associates in the UK to perform site monitoring and management tasks essential for clinical studies. The role requires a minimum of two years of on-site monitoring experience and a strong understanding of clinical research regulations

Job Summary

  • The role involves performing selection, initiation, monitoring, and close-out visits to ensure sites conduct studies according to the protocol and regulations.
  • Candidates will work with sites to adapt and drive subject recruitment plans while managing regulatory submissions and data query resolution.
  • IQVIA is a leading global provider of clinical research services committed to integrity and accelerating the development of innovative medical treatments.

Matching Summary

Match Score: 85

IQVIA is seeking experienced Senior Clinical Research Associates in the UK to perform site monitoring and management tasks essential for clinical studies. The role requires a minimum of two years of on-site monitoring experience and a strong understanding of clinical research regulations.

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) knowledge
  • Site monitoring visit execution
  • Subject recruitment plan management
  • Trial Master File maintenance
  • Protocol adherence evaluation

Nice-to-have

  • Strong problem-solving skills
  • Effective time management abilities
  • Collaborative team working style

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 2 years of on-site monitoring experience
  • Not eligible for UK visa sponsorship

Work Rights

Must have UK work authorization

Tailored Resume

Cover Letter