CTA 1 - One Sponsor dedicated- Prague
Core
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and clinical documentation management.
Role type
Administrative Specialist (Clinical Research)
Builds
Trial Master Files (TMF), clinical documentation, and study file tracking
Domain
Clinical Research / Life Sciences
Deliverable
dashboards & analysis
Required skills
Administrative support, Clinical Trial Supplies tracking, Case Report Forms (CRFs) management, Microsoft Office (Word, Excel, PowerPoint), GCP/ICH guidelines knowledge, English language proficiency
Preferred skills
Site visit accompaniment experience
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, serve as central contact for project communications
Seniority
Mid-level, individual contributor
