Clinical Trials Assistant
Core
Administrative support for Clinical Research Associates and Regulatory teams, managing clinical documentation, trial supplies, and data flow.
Role type
Administrative Clinical Trials Assistant
Builds
Clinical Trial Master Files (TMF), study files, and clinical data packages
Domain
Clinical research / Life sciences
Required skills
Clinical trial documentation management, Case Report Form (CRF) tracking, Clinical Trial Supply management, Regulatory guideline awareness (GCP/ICH), Microsoft Office proficiency, English language proficiency
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, Act as central contact for project communications
Seniority
Junior, 2+ years experience
