Clinical Trial Assistant - Based in Spain
Core
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and site compliance tracking.
Role type
Clinical Trial Assistant
Builds
Trial Master Files (TMF) and clinical documentation systems
Domain
Clinical research / Life sciences
Deliverable
dashboards & analysis
Required skills
Clinical document management, Case Report Form (CRF) tracking, Clinical Trial Supply management, Regulatory guideline awareness (GCP/ICH), Microsoft Office proficiency
Preferred skills
Life science degree, prior Clinical Trials Assistant experience
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 CRF queries and data flow, act as central contact for project communications
Seniority
Entry-level to Junior
