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Job Description & How to Apply Below
A global biopharmaceutical solutions organization is seeking a Principal Medical Writer to develop regulatory documents such as Clinical Study Reports and Clinical Summaries. The ideal candidate will have strong experience in regulatory document development and project management, with eCTD submission experience preferred. This remote role emphasizes collaboration with cross-functional teams and does not require mentoring of junior writers. The position is geared towards professionals passionate about enhancing patient outcomes.
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Position Requirements
10+ Years
work experience
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