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Clinical Research Associate

2 months ago


Melbourne, Victoria, Australia IQVIA Argentina Full time
About the Role

We are seeking a highly experienced Senior Clinical Research Associate to join our team at IQVIA Argentina. This role is ideal for individuals with a strong background in clinical research and a passion for delivering high-quality results.

Key Responsibilities
  1. Site Management: Perform site selection, initiation, monitoring, and close-out visits to ensure compliance with regulatory requirements and study protocols.
  2. Monitoring and Quality Assurance: Provide monitoring visits and site management for various protocols, sites, and therapeutic areas, evaluating the quality and integrity of study site practices.
  3. Communication and Collaboration: Administer protocol and related study training to assigned sites, establish regular lines of communication, and collaborate with study team members for project execution support.
  4. Documentation and Reporting: Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans, ensuring accurate and timely reporting.
Requirements
  1. Education: Bachelor's degree in Life Sciences or other scientific/nursing disciplines.
  2. Experience: Minimum of 4 years independent site monitoring experience, with a strong background in clinical research and a proven track record of delivering high-quality results.
  3. Skills and Knowledge: Extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, with the ability to travel on a regular basis and work in a fast-paced environment.

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 a meaningful impact and create a healthier world.