Description
The Source Document Specialist creates, maintains, reviews, and approves study source documents; maintains version control; coordinates with study teams, vendors, sponsors, coordinators, and investigators; ensures compliance with GCP, FDA, and sponsor requirements; supports audit preparation; and provides training and workflow improvements. The role reports to the Source Document Team Lead, is non-exempt, and may require occasional weekend or overtime hours. At least six months of medical experience is desired, along with strong communication, attention to detail, task management, and English fluency.
