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About the Role:
- Serve as lead author on regulatory documents and provide strategic program-level input.
- Own client relationships and drive high-quality deliverables.
- Mentor other writers and help develop AI-optimized workflows.
Key Requirements:
- At least 5 years of medical writing experience in pharma, biotech, or CRO.
- Expertise in writing CSRs, protocols, IBs, and submission documents.
- Strong project management and independent work skills.
Why Join Us:
- Fully remote with flexible hours and competitive compensation.
- Direct client access and opportunities for leadership.
- Supportive team culture focused on quality and continuous learning.
Eldridge Writing
Eldridge Writing provides top-tier medical writing services to pharmaceutical and biotechnology clients. We are a small, collaborative team that values quality and serves as a true extension of our clients’ teams.