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Our company is located in Japan. We specialize in clinical research and provide medical writing services including manuscript developments for academic journal submissions, to ultimately achieve publications.
Work in a matrix team to ensure delivery of high quality, fit-for-purpose clinical documents that accurately reflect associated data, and are in line with GSK standards and global, regional and/or local regulatory requirements.
To write, review and/or manage the production of high-quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications.
As part of our on-going growth, we are currently recruiting for a Senior / Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North America and Asia Pacific.
The Council of Europe and its European Directorate for the Quality of Medicines & HealthCare (EDQM) are looking for enthusiastic and rigorous scientific assistants with an excellent command of English (mother tongue level) to join our European Pharmacopoeia Department.