Sr Reg Doc Coord

1. Assist authors with the finalization of their clinical documents according to International Research and Development Document Standards (IRDDS), reflected in Novstyle 
2. Review content final clinical documents to assure Novstyle compliance within electronic document management systems (eDMS) finalization 
3. Provide guidance during the document life-cycle in eDMS towards finalization 
4. Maintain record (editors log) to track the flow of documents that are edited and finalized in the eDMS. 
5. Provide training to associates on Novstyle editing and relevant document management processes 
6. Act as eDMS superuser; solve or escalate eDMS and Novstyle issues 
7. Operationally support document management activities (e.g. external document QC organization, including batch export of document data sources from CREDI, categorization and quantification of QC findings) 
8. Metrics reports (e.g. mandatory trainings, metrics).

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.