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Senior Manager, Medical Writing
Teva Pharmaceuticals • West Chester, PA, US • published 2026-10-03 03:13:59.997725
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**We Are Teva** --------------- We’re Teva, a leading innovative biopharmaceutical company, enabled by a world\-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high\-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high\-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.**Our Team, Your Impact** ------------------------- A Sr. 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. **How You’ll Spend Your Day** ----------------------------- * Primarily works at a project level. * Writes and edits clinical regulatory documents including study reports, protocols, briefing books, inv...
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