Clinical Research Associate

22 hours ago

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

IQVIA Argentina is seeking a 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.

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.
  • Collaborate and liaise with study team members for project execution support as appropriate.
Requirements
  • Experience of independent on-site monitoring in Argentina.
  • Monitoring experience of Oncology, Cardiovascular, Respiratory, Diabetic, Immunology, or Renal therapeutic areas.
  • Life science degree educated or equivalent industry experience.
  • Valid driver's license and access to vehicle, and flexibility to travel to sites as required.

This role is not eligible for Argentina visa sponsorship.

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