Clinical Research Associate

14 hours ago


Reading, Reading, United Kingdom IQVIA Argentina Full time
Job Summary

IQVIA Argentina is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and evaluating the quality and integrity of study site practices.

Key Responsibilities
  • Perform site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements.
  • Work with sites to adapt and drive subject recruitment plans to enhance predictability.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution.
  • Ensure copies/originals of site documents are available for filing in the Trial Master File and verify that the Investigator's Site File is maintained in accordance with GCP and local regulatory requirements.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans.
Requirements
  • Experience of independent on-site monitoring in the UK.
  • Monitoring experience of Oncology, Cardiovascular, Respiratory, Diabetic, Immunology, or Renal therapeutic areas.
  • Life science degree educated or equivalent industry experience.
  • UK driving license and access to vehicle (excluding London travel zones 1 & 2) and flexibility to travel to sites as required.

This role is not eligible for UK visa sponsorship.



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