Trial Master File & Regulatory Docs Specialist
FATHOM LIFE SCIENCES & TECHNOLOGY SERVICES
FATHOM LIFE SCIENCES & TECHNOLOGY SERVICES is seeking a detail-oriented Clinical Trial Document Manager to set up and maintain the local Trial Master File (TMF) and Investigator Site File (ISF) in line with ICH/GCP and local requirements, and to support the CRA. You will create/import regulatory documents into GEL, ensure template/version compliance, and assist with electronic submissions and training of others on study administration. #J-18808-Ljbffr FATHOM LIFE SCIENCES & TECHNOLOGY SERVICES
Vacancy posted 3 days ago
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