DUTIES & RESPONSIBILITES 1.Planning, writing, and management of regulatory documents, e.g. clinical trial reports etc. 2.Planning, writing, and management of manuscripts, abstracts, posters and other medical publications 3.Contribute to related clinical documents (e.g. study protocols, analysis plans, statistical outputs etc.) 4.Ensure the quality of assigned medical writing projects JOB REQUIREMENTS 1.At least master degree in biomedical sciences/pharmacy/medicine or related fields 2.At least 3 years of work experience in medical writing or clinical research 3.English skills: CET-6 or above 4.Location: Shanghai
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