Sr CTA - Sponsor Dedicated - Israel
Core
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and clinical documentation management.
Role type
Senior Clinical Trial Assistant (CTA)
Builds
Trial Master Files (TMF), clinical documentation, and clinical trial supply tracking
Domain
Clinical Research / Life Sciences
Required skills
Clinical Trial Assistant experience, Clinical Research experience, Microsoft Office (Word, Excel, PowerPoint), GCP/ICH guidelines knowledge, Protocol requirements knowledge
Preferred skills
Site visit accompaniment experience
Responsibilities
Update and maintain clinical documents and systems (e.g., TMF), prepare and archive clinical documentation and reports, review study files for completeness, coordinate tracking of Clinical Trial Supplies and Case Report Forms (CRFs), act as central contact for project communications
Seniority
Senior, hands-on IC
