Clinical Document Administrator

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: 
- Assist authors with the finalization of their clinical documents according to International Research and Development Document Standards, reflected the internal document-template 
- Review content final clinical documents to assure the document-template compliance towards the document management system finalization.
- Provide guidance during the document life cycle in the system towards finalization.
- Maintain record (Editors Log) to track the flow of documents that are edited and finalized in the system.
- Provide training to associates on internal document-template editing and relevant document management processes.
- 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 systems 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).