Clinical Trial Assistant, HYBRID in Wilmington, DE
Core
Administrative support for clinical research teams, managing trial documentation, supplies, and data flow to ensure site compliance and project timelines.
Role type
Clinical Trial Assistant
Builds
Clinical Trial Master Files (TMF), clinical documentation, and supply tracking systems
Domain
Clinical Research / Life Sciences
Required skills
Clinical Trial Master File (TMF) management, Case Report Form (CRF) tracking, clinical supply chain management, regulatory guideline awareness (GCP/ICH), Microsoft Office proficiency, study file review
Preferred skills
None stated
Technologies
Microsoft Word, Excel, PowerPoint
Responsibilities
Update and maintain clinical documents and systems, prepare and archive clinical documentation, review study files for completeness, track clinical trial supplies, manage CRFs and clinical data flow, act as central contact for project communications
Seniority
Mid-level, hands-on support
