Clinical Trial Assistant
Core
Support Clinical Research Associates and Regulatory teams in maintaining clinical documents, managing trial supplies, and tracking clinical data flow to ensure site compliance and project timelines.
Role type
Clinical Trial Assistant
Builds
Clinical Trial Master Files (TMF), clinical documentation, and trial supply tracking systems
Domain
Clinical research / Life sciences
Required skills
Clinical document management, Case Report Form (CRF) tracking, Clinical Trial Supply management, Regulatory guideline awareness (GCP/ICH), Microsoft Office proficiency, Project timeline management
Preferred skills
Site visit accompaniment experience, Protocol knowledge
Responsibilities
Update and maintain clinical documents and systems, Prepare and archive clinical documentation, Review study files for completeness, Track and manage clinical data flow and queries, Act as central contact for project communications
Seniority
Mid-level, hands-on support