Job Summary
A company is looking for a Medical Writer to create and manage clinical documents for regulatory submissions and client communication.
Key Responsibilities
- Gather, analyze, and prepare clinical documents for regulatory submission and internal use
- Serve as primary client contact for medical writing projects, managing timelines and resolving issues
- Ensure document quality and compliance with regulatory guidelines and standard operating procedures
Required Qualifications
- Extensive clinical/scientific writing skills
- Proven ability to use Microsoft Office products (including Word, Excel & PowerPoint)
- Experience in managing multiple tasks in a fast-paced environment
- Knowledge of FDA/EMA regulatory guidelines
- Ability to work independently and demonstrate initiative
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