Clinical Trials Associate (US)

Clinical Trials Associate provides administrative and project tracking support to clinical project teams, managing document workflows, system access, and quality control for assigned trials across multiple sites.

Responsibilities

• Arrange and track system access for project team members across clinical sites
• Maintain and audit documentation on project portals to ensure current versions
• Coordinate preparation and shipment of trial documentation including Investigator Site Files
• Manage version control and quality assurance of project documents for trial master file
• Track and maintain project information including site medical question and answer logs

Requirements

• Bachelor's degree or equivalent professional experience
• Minimum one year experience in a related clinical or administrative role
• Fluent English and local language proficiency for assigned location
• Proficiency in MS Office applications (Outlook, Word, Excel, PowerPoint)
• Strong attention to detail and quality focus
• Ability to manage multiple concurrent tasks independently

Compensation: $16.83 - $33.65 annually (hourly rate equivalent)