Clinical Trial Assistant

Job Summary

Supporting the planning and execution of clinical research studies, the full-time Clinical Trial Assistant will manage documentation, ensure compliance with regulatory standards, and coordinate communication among study teams while working remotely.

Key responsibilities

• Assists in the preparation and maintenance of clinical trial documentation, including Trial Master Files and Investigator Site Files
• Tracks study-related documents to ensure completeness and compliance with regulatory standards
• Coordinates communication between study teams, sponsors, and investigational sites

Required qualifications

• Bachelor's degree in life sciences, healthcare, or a related field (preferred)
• 1-2 years of experience in clinical research
• Knowledge of clinical research processes and regulations, including ICH-GCP guidelines
• Working knowledge of CTMS and e-TMF or e-ISF systems
• Proficiency in Microsoft Office applications