Main Responsibilities:
1. Proof-reading and copy-editing in English, and formatting in MS Word
2. Handling the review cycle and tracking versions of draft documents
3. Preparing and compiling multiple-component reports and submissions
4. Communicating document status and progress to stakeholders
5. Electronic publishing of final Word documents as eCTD-compliant PDFs using Adobe Acrobat and ISI Toolbox
6. Updating of existing and creating new internal processes, templates, guidelines and instructions
7. Providing training to clinical authors and other colleagues handling documents
Qualifications and Experience:
8. Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required
9. A scientific degree
10. English mother tongue
11. Experience in editing/proof-reading or publishing
12. Knowledge of the pharmaceutical industry and drug development a plus