Senior Medical Writing Manager
1 week ago
We are seeking a highly skilled Senior Medical Writing Manager to join our team at Lexeo Therapeutics. As a key member of our cross-functional team, you will be responsible for generating and leading the development of Clinical and Regulatory documents across all LEXEO programs.
Key Responsibilities:
- Document Development: Draft or contribute to the development of high-quality submission-ready documents, including protocols, protocol amendments, clinical study reports, and other regulatory documents.
- Quality Assurance: Ensure the quality of deliverables by conducting editorial review of documents and completing or managing the quality checking of documents according to LEXEO standards.
- Project Management: Manage the document development process for deliverables, including planning, project execution, and project finalization.
- Collaboration: Build and maintain collaborative relationships with cross-functional internal subject matter experts and external partners.
Requirements:
- Education: A graduate-level education is required.
- Experience: A minimum of 7 to 10 years of experience with related work within a pharmaceutical/biotech company or CRO is required.
- Skills: Positive and proactive written and verbal communication skills, ability to manage multiple projects simultaneously, and proficiency in Microsoft Office Suite are required.
About Lexeo Therapeutics:
Lexo Therapeutics is a clinical stage genetic medicine company dedicated to transforming healthcare by applying pioneering science to fundamentally change how genetically defined cardiovascular diseases and APOE4-associated Alzheimer's disease are treated.
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