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Clinical Research Associate

2 months ago

Reading, Reading, United Kingdom IQVIA Argentina Full time
{"title": "Clinical Research Associate", "content": "Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for conducting site monitoring visits, ensuring compliance with regulatory requirements, and collaborating with study team members to drive project execution.

Key Responsibilities
  • Perform site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability
  • Administer protocol and related study training to assigned sites and establish regular lines of communication
  • Evaluate the quality and integrity of study site practices and escalate quality issues as appropriate
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution
Requirements
  • Life science degree education
  • Independent on-site monitoring experience
  • Experience handling multiple protocols and sites across various drug indications
  • Flexibility and ability to travel
  • Strong communication, written, and presentation skills
About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.

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