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Join us on our journey of pivot to strategic growth:
• To make an impact, innovate, and work on diverse portfolio of products within a promising pipeline centered around our core therapeutic areas
• To help make healthcare accessible to more patients, as part of a highly global diverse matrixed R&D team,
• To improve health and enable people to live better, healthier lives.
A Manager, in Global Regulatory Medical Writing, writes and edits clinical regulatory documents, including submission summaries and other complex documents, provides basic-level oversight and guidance, as well as resource management for the direct medical-writing support in the production of clinical research documentation used in drug development and product registrations.
Travel Requirements:International and domestic
US-Based Remote (US Eastern time zone preferred)
Therapy Area Head, Medical Writing
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