Clinical Research Associate

4 weeks ago


Reading, Reading, United Kingdom Pharmiweb Full time

Job Summary

IQVIA UK is seeking an experienced Clinical Research Associate to strengthen our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and ensuring the quality and integrity of study site practices.

Key Responsibilities

  • Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements.
  • Work with sites to adapt and drive subject recruitment plans.
  • Administer protocol and related study training to assigned sites.
  • Evaluate the quality and integrity of study site practices.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals.
  • Ensure site documents are available for filing in the Trial Master File.
  • Create and maintain documentation regarding site management and monitoring visit findings.

Requirements

  • Experience of independent on-site monitoring in the UK.
  • Life science degree educated or equivalent industry experience.
  • Flexibility to travel to sites as required.

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



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