Les offres d'emploi : Professions sociales - Santé ...

Key Responsibilties:

- Experience of document management technology and electronic publishing software.
- Responsible for the compilation and publishing of regulatory submissions using electronic publishing software or paper-based system.
- Process electronic files incorporating bookmarks, hyperlinks, tabs and other formatting requirements.
- Using electronic publishing tools to compile and publish electronic regulatory submissions (e.g., clinical trial applications, briefing books, Marketing Authorisation Applications).
- Contributing to the development, implementation and support of regulatory publishing systems in Europe.
- Developing and implementing e-templates for European submission documents.
- Assisting in the dispatch of regulatory submissions in electronic format.
- Assisting in the review and maintenance of relevant guidelines and SOPs.
- Working closely with the Regulatory Operations Group in Summit, USA, to ensure consistent methods of filing and publishing.
- Archiving of European regulatory documents within electronic document management system (e-sub Live Link).
- Assist and support Regulatory team on any other activities related to the above.

Your Profile:

- Possess university degree or higher in the Life Sciences.
- Prior experience in data management within the pharmaceutical sector.
- Possess excellent technical competence.
- Ability to work individually as well as in a team.
- Possess excellent administrative skills, attention to detail and to deliver within the timeline.
- Ability to communicate effectively in a multi- cultural and multi functional-environment.


MICHAEL PAGE...