Clinical Trial Assistant - Hybrid

Role Overview: The Clinical Trial Assistant supports clinical research operations by managing trial documentation, clinical supplies, and site monitoring activities in a hybrid setting. Key Responsibilities Maintain and update clinical documents and Trial Master File systems for compliance.Prepare, handle, distribute, and archive clinical documentation according to procedures.Track and manage Case Report Forms, queries, and clinical data flow.Assist with handling and distributing clinical trial supplies and tracking information.Act as a central communication point for project correspondence and documentation. Qualifications & Skills Bachelor's degree.Minimum of 3 years of administrative support experience.Proficiency in Microsoft Word, Excel, and PowerPoint.Excellent written and verbal English communication skills.Strong organizational and time management skills.Knowledge of GCP and ICH guidelines and understanding of clinical protocol requirements (training provided).