Regulatory Compliance Specialist

5 days ago


Reading, Reading, United Kingdom IQVIA Argentina Full time

About the Position

We are looking for a skilled Clinical Research Associate to join our dynamic team at IQVIA Argentina. As a CRA, you will be responsible for monitoring trial sites, managing subject recruitment plans, and ensuring compliance with regulatory requirements.

Requirements

  • Life science degree education required
  • Experience in independent on-site monitoring essential
  • Familiarity with GCP and ICH guidelines necessary
  • Excellent communication, written, and presentation skills

About Our Company

IQVIA is a global leader in providing advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our mission is to push the boundaries of human science and data science to make a positive impact in the world.



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