Clinical Research Specialist

2 days ago


Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

Role Summary:

A Clinical Research Specialist is needed to drive site activation and customer experience across the globe.

This individual will review documents for completeness and accuracy, prepare site regulatory documents, and track document progress, approval, and execution.

In this role, you will be responsible for reviewing regulatory documents, distributing completed documents to sites and internal project team members, and maintaining accurate information in internal systems and databases.

Main Responsibilities:

  1. Reviewing documents for completeness and accuracy under senior staff guidance
  2. Preparing site regulatory documents
  3. Tracking document progress, approval, and execution


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