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Responsibilities Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. Represent Tech Writing and Document management
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Excellent writing and editing skills with the ability to convey complex scientific information clearly and concisely. The ideal candidate will have 4-8 years of experience in regulatory medical writing and a strong background in drafting essential regulatory documents, including Investigator’s Bro
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