Source Document Specialist
Company: VirtualVocations
Location: Vista
Posted on: May 24, 2025
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Job Description:
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
Keywords: VirtualVocations, Los Angeles , Source Document Specialist, Other , Vista, California
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