Clinical Document Administrator

Beschreibung

Referenz Nr.: 8858TG
Branche: Pharmaceutical
Einsatzort: Basel
Beginn: asap
Dauer: 6 months +
Introduktion: Take ownership and edit clinical registration documents within a document management system, according to International Research and Development Document Standards, as reflected by the internal developed document-template. Further assist end-users as document management system super users in their efforts to overcome challenges with this system.
Rolle: 1. Assist authors with the finalization of their clinical documents according to International Research and Development Document Standards, reflected the internal document-template 2. Review content final clinical documents to assure the document-template compliance towards the document management system finalization. 3. Provide guidance during the document life-cycle in the system towards finalization. 4. Maintain record (Editors Log) to track the flow of documents that are edited and finalized in the system. 5. Provide training to associates on internal document-template editing and relevant document management processes. 6. May act as a system super user; solve or escalate system and document-template issues.
Anforderungen: -Medical or scientific education desirable. - Excellent word processing skills with MS Word. - Strong communicator with customer focus. - Good experience working with Microsoft office - Global, cross-cultural perspective and customer orientation. - Experience with clinical document management sytems is of great advantage. - Good knowledge of clinical registration documentation is helpful. - A basic understanding of clinical drug development process and familiarity with medical terminologies is a plus.
Sprachen: Fluent English (oral and written).