Clinical Trial Associate

About the role

The Clinical Trial Associate serves as the primary point of contact for administrative support to the site and clinical trial team. The Clinical Trial Associate is also responsible for coordinating the day to day clinical study activities and maintaining the logistical aspects of clinical trials in compliance with protocol, International Council for Harmonisation guideline for Good Clinical Practice (ICH-GCP), local regulations, applicable Standard Operating Procedures (SOPs) and project-specific requirements.

Responsibilities

• Primary Trial Master File Duties
  • Assume primary responsibility for the setup, development, maintenance, and correspondence of the Trial Master File (TMF) for studies assigned
  • Set up and maintain electronic filing systems/set up of the Invest