Descripción del trabajo
The Clinical Study Report (CSR) Document Specialists is responsible to populate, track, QC and perform technical editorial checks of the CSR appendices for assigned studies, from authoring until document finalization in the DMS in compliance with current Novartis processes, ICH-GCP, and relevant regulatory requirements. CSR Document specialists responsibilities include, but are not limited to: Lead the CSR appendices kick off meeting and define the timelines together with the CSR sub team Plan …