Job Summary
A company is looking for a Medical Writing Word Processing Coordinator II.
Key Responsibilities
- Format, proof, and manage clinical regulatory documents to ensure they are submission-ready
- Communicate with colleagues regarding timelines and document completion dates
- Maintain document tracking and ensure compliance with eSubmissions standards
Required Qualifications
- Minimum of 3 years of relevant industry experience in medical writing
- Experience in a global pharma, biotech, or life sciences organization
- Knowledge of eSubmissions styles and formatting standards
- Ability to perform literature searches and ensure correct citations
- Familiarity with regulatory submission processes and requirements
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