Clinical Document Agent

About the role

This role focuses on transforming raw study data into structured electronic documents while ensuring compliance with established procedures and quality standards. You will contribute to the preparation of patient files, clinical documentation forms, and essential study records. Working closely with Clinical Study Managers and cross-functional teams, you will help ensure that documentation is complete, accurate, and delivered within project timelines.

What you'll do

• Prepare and manage subject files throughout clinical projects, including reviewing templates, checking documentation accuracy, meeting deadlines
• Create electronic clinical documentation forms and prepare source documentation using Microsoft Excel and other relevant tools
• Convert raw clinical study data into electronic formats while ensuring accuracy, consistency, and compliance with established procedures
• Review and validate clinical documentation before transcription, identifying and correcting errors to maintain high-quality records
• Calculate final blood volumes for study participants and verify that appropriate washout periods and dates are correctly documented

What you need

• 1–3 yrs of experience
• Clinical research
• MS Office
• SOP writing
• Problem solving
• Transcription
• M.Sc