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, clinical documentation, and study files
Domain
Clinical research / Life sciences
Required skills
Clinical Trial Assistant experience, GCP/ICH guidelines knowledge, Case Report Form (CRF) management, Clinical Trial Supplies tracking, Microsoft Office proficiency, English/Spanish fluency
Preferred skills
Life science degree
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 queries, act as central contact for project communications
Seniority
Entry-level to Junior
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