ID oferty: 1624413
Źródło: adzuna
Kategoria: Praca naukowa i QA
Opis: Job Overview The Clinical Study Report (CSR) Document Specialist is responsible forthe coordination, formatting, quality control, document management, and finalization of Clinical Study Report appendices for assigned studies. This role works closely with TMF Managers, Study Leads, Medical Writers, Biostatisticians, Clinical Operations, Regulatory Affairs, Data Management, and Quality teams to ensure that clinical study documentation is accurate, compliant, submission-ready, and delivered accord…
Wynagrodzenie min: 2.058e+06
Wynagrodzenie max: 3.822e+06
Utworzono: 25.09.2026 19:46