Clinical Trials Associate - Australia - Remote

📋 Description

• • As a Clinical Trials Associate at Worldwide Clinical Trials, you will provide essential administrative and project tracking support to clinical project teams, ensuring timely and accurate execution of tasks for assigned projects with Project Delivery services.
• • Your day-to-day responsibilities include arranging and tracking system access for project team members, maintaining and quality auditing document revisions on project portals, assisting with preparation and shipment of clinical trial documentation such as Investigator Site Files, maintaining version control of project documentation, and submitting materials to the trial master file.
• • You will also assist in tracking and maintaining project-related information, including site medical question and answer logs, contributing to the smooth operation of clinical trials across global studies.
• • Worldwide Clinical Trials is a global midsize CRO with over 3,500 experts dedicated to improving lives through innovative, high-quality clinical research. The company fosters a diverse, inclusive, and collaborative environment where employees are empowered to thrive and do their best work every day.
• • In this role, you will develop strong organizational, administrative, and documentation management skills within the clinical trials lifecycle, gain hands-on experience in project support functions, and build expertise in regulatory-compliant processes—positioning you for growth in clinical research operations or project coordination.