Lead impactful medical writing operations for submission-ready documents. Collaborate with cross-functional teams in a dynamic regulatory environment. Develop tools, templates, and training materials to enhance operations.
Manager, Medical Writing Operations
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Manage medical writing operations to ensure submission-ready documents meet high-quality standards and regulatory requirements.
- Support document formatting, consistency, publishing, and archiving within central file systems.
- Collaborate with cross-functional teams to compile and publish CSR appendices.
- Perform quality control checks for electronic publishing, hyperlinks, and bookmarks.
- Develop and maintain tools, templates, and training materials for medical writing operations.
- Support vendor oversight and training for internal staff and external contractors.
- Assist with CSR shells and preparation of in-text tables and figures.
- Ensure compliance with global regulatory requirements and internal best practices.
Key Responsibilities & Duties
- Collaborate across functions to collect, compile, and publish CSR appendices.
- Perform electronic publishing QC, including hyperlinks and bookmarks, ensuring submission readiness.
- Format MS Word submission components per style and regulatory requirements.
- Serve as SME for format QC, submission readiness, and document management systems.
- Ensure documents are stored and archived appropriately in EDMS and eTMF systems.
- Support creation and updates of templates, style guides, and tools.
- Perform administrative tasks to support projects and operational needs.
- Assist with training internal staff and external contractors/CROs.
Job Requirements
- Bachelor’s degree in a relevant scientific or technical field.
- 4+ years of experience in biotech/pharma or CRO document QC and publishing.
- Strong understanding of health authority/ICH PDF and eCTD requirements.
- Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Windows.
- Experience with electronic document management systems.
- Ability to manage multiple projects in a deadline-driven environment.
- Exposure to StartingPoint templates, SharePoint, EndNote, and Toolbox Pharma preferred.
- Alignment with core values: Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture, and Passion for Excellence.
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