Clinical Trial Associate

hace 3 semanas


Xico, México Icon A tiempo completo

Role Overview

As a Clinical Trial Associate at ICON, you will be part of a world-leading clinical research organization. This role involves supporting the Local Trial Manager and CRA to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution, and closing of clinical trials. You will be responsible for regulatory document review and approval, including site-specific Informed Consents. Ensuring trial-related activities are in compliance with GCO SOPs, policies, and local regulatory requirements.

Key Responsibilities

  • Work with the Local Trial Manager and CRA to ensure overall site management and adherence to internal SOPs, policies, and local regulatory requirements.
  • Maintain site-level protocol information in Trial Management Systems (e.g. CTMS).
  • Ensure current versions of the required trial documents, trial-related materials, and supplies are provided to the investigational site within required timeframes.
  • Provide current and complete documents requested by the IEC/IRB and HA.
  • Distribute, collect, review, and track regulatory documents, agreements, and training documentation.
  • Contribute to process improvement initiatives.

Requirements

  • 1-2 years of experience in a clinical trial setting.
  • A minimum of a BA degree.
  • Strong knowledge of MS Office.
  • Excellent organizational skills and ability to collaborate and handle multiple priorities within a matrix environment.

What ICON Offers

Our success depends on the quality of our people. We offer a range of benefits, including annual leave entitlements, health insurance, and retirement planning offerings.


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