Source Document Specialist

A company is looking for a Source Document Specialist to create and manage source documents for clinical trials. Key Responsibilities Create and maintain accurate versions of source documents in compliance with GCP Guidelines and internal SOP Review and update source documents based on protocol amendments and ensure they are equipped to record required data Manage communication with site staff and organize, file, and archive source documents for each clinical trial Required Qualifications, Training, and Education Bachelor's degree in a relevant field (Life Sciences, Healthcare, or related discipline) or equivalent experience Experience as a Clinical Research Coordinator with diverse clinical trials preferred Proficiency in e-Source build and design, as well as creation and revision of paper source templates Ability to interpret clinical trial protocols to design accurate source documents Self-motivated and highly organized individual capable of working independently

Apr 26, 2025 - 01:04

A company is looking for a Source Document Specialist to create and manage source documents for clinical trials. Key Responsibilities Create and maintain accurate versions of source documents in compliance with GCP Guidelines and internal SOP Review and update source documents based on protocol amendments and ensure they are equipped to record required data Manage communication with site staff and organize, file, and archive source documents for each clinical trial Required Qualifications, Training, and Education Bachelor's degree in a relevant field (Life Sciences, Healthcare, or related discipline) or equivalent experience Experience as a Clinical Research Coordinator with diverse clinical trials preferred Proficiency in e-Source build and design, as well as creation and revision of paper source templates Ability to interpret clinical trial protocols to design accurate source documents Self-motivated and highly organized individual capable of working independently