Clinical Research Associate

22 hours ago

Reading, Reading, United Kingdom IQVIA Argentina Full time
Drive Healthcare Forward with IQVIA

Our Sponsor Dedicated (cFSP) team is growing, and we're seeking a talented Clinical Research Associate to join our mission to drive healthcare forward.

About the Role

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 administering protocol and related study training. You will also evaluate the quality and integrity of study site practices and manage the progress of assigned studies.

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
  • 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

This role is not eligible for UK visa sponsorship. 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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