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Clinical Research Associate

2 months ago

Reading, Reading, United Kingdom IQVIA, Inc. Full time

About the Role

We are seeking a skilled Clinical Research Associate to join our dedicated team at IQVIA, Inc. As a key member of our team, you will play a vital role in driving the success of our clinical trials.

Key Responsibilities

  • Conduct site monitoring visits to ensure compliance with regulatory requirements and contracted scope of work.
  • Work with sites to develop and track subject recruitment plans to enhance predictability.
  • Administer protocol and related study training to assigned sites and establish regular communication to manage project expectations and issues.
  • Evaluate site practices and escalate quality issues as necessary.
  • Manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
  • Ensure accurate documentation of site management, monitoring visit findings, and action plans.

Requirements

  • Life science degree education.
  • Experience in independent on-site monitoring.
  • Flexibility and ability to travel.

About IQVIA, Inc.

IQVIA, Inc. is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We strive to make a meaningful impact on human health by pushing the boundaries of human science and data science.