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Clinical Research Associate

2 months ago

Reading, Reading, United Kingdom IQVIA Argentina Full time
About the Role

We are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a Clinical Research Associate, you will play a critical role in the execution of clinical trials, ensuring the quality and integrity of study site practices.

Key Responsibilities
  • Site Management
    • Perform site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements.
    • 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.
  • Monitoring and Compliance
    • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
    • Escalate quality issues as appropriate and ensure that site documents are available for filing in the Trial Master File (TMF).
  • Study Execution
    • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
    • Collaborate and liaise with study team members for project execution support as appropriate.
Requirements
  • You should be life science degree educated.
  • You have experience of independent on-site monitoring experience.
  • You've handled multiple protocols and sites across a variety of drug indications.
  • Flexibility and ability to travel.
  • Strong communication, written, and presentation skills.
About IQVIA Argentina

IQVIA Argentina 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.