Clinical Trials Assistant
Core
Assist Clinical Research Associates and Regulatory teams in maintaining clinical documents, systems, and trial supplies to ensure site compliance and performance.
Role type
Administrative support specialist for clinical trials
Builds
Clinical Trial Master Files (TMF), study files, and clinical data flow
Domain
Clinical research / Life sciences
Required skills
Clinical trial administration, document management, case report form (CRF) tracking, supply chain tracking, regulatory guideline awareness (GCP/ICH), Microsoft Office proficiency
Preferred skills
Site visit accompaniment experience
Technologies
Microsoft Word, Excel, PowerPoint
