Clinical Trial Assistant
Core
Administrative support for Clinical Research Associates and Regulatory teams to maintain Trial Master Files, manage clinical documentation, and track trial supplies.
Role type
Clinical Trial Assistant
Builds
Trial Master Files, clinical documentation packages, and supply tracking records
Domain
Clinical research / Life sciences
Deliverable
dashboards & analysis
Required skills
Clinical research administration, Trial Master File (TMF) management, clinical documentation handling, Case Report Form (CRF) tracking, regulatory guideline awareness (GCP/ICH), Microsoft Office proficiency
Preferred skills
Site visit accompaniment, regulatory submissions experience
Responsibilities
Update and maintain clinical documents and systems, prepare and archive clinical reports, review study files for completeness, track clinical trial supplies, manage CRF queries and data flow, serve as central contact for project communications
Seniority
Entry-level to Junior
