Job Description
Liam Newton has partnered with a mid-sized Biopharma who are searching for a Senior Manager of Medical Writing.
This business has a range of products already commercialized and has a robust pipeline across various Therapeutic Areas.
This company is committed to long-term career development and can offer a very strong salary package.
Responsibilities:
1. Produce high-quality and on-time Regulatory documents.
2. Facilitate/manage efficient review and editing process for documents produced internally and/or externally by consultants, contractors, and vendors.
3. Collaborate cross-functionally with other departments such as Biometrics, Clinical Operations, Clinical Development, Regulatory Affairs, Pre-Clinical Development, Program Management, Research, Quality, and Corporate Communications, as well as with external stakeholders.
4. Serve as subject matter expert for clinical documents and their production.
5. Contribute to SOP and template development and maintenance.
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