Clinical Research Documentation Administrator (TMF)
Core
Managing the Trial Master File (TMF) to ensure data integrity and document quality for clinical trials.
Role type
Clinical Research Documentation Administrator (TMF)
Builds
Regulatory-compliant clinical trial documentation packages
Domain
Clinical Research / Biopharmaceuticals
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Electronic filing system management, document tracking and maintenance, quality assurance checks, global communication, document preparation for shipment
Preferred skills
Bachelor's degree, document administration experience
Technologies
MS Office
Responsibilities
Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; Prepare documents for shipment
Seniority
Entry-level to Mid-level, hands-on IC