CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking a:Documentation Specialist in Regulatory Affairsfor a contract of 12 months, based in Basel.Main Responsibilities:
Proof-reading and copy-editing in English, and formatting in MS Word
Handling the review cycle and tracking versions of draft documents
Preparing and compiling multiple-component reports and submissions
Communicating document status and progress to stakeholders
Electronic publishing of final Word documents as eCTD-compliant PDFs using Adobe Acrobat and ISI Toolbox
Updating of existing and creating new internal processes, templates, guidelines and instructions
Providing training to clinical authors and other colleagues handling documents
Knowledge of the pharmaceutical industry and drug development a plus
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