Job Summary
A healthcare company has an open position for a Remote Clinical Principal Regulatory Writer.
Core Responsibilities of this position include:
- Serving as liaison and subject matter expert internally and for clients
- Authoring documents per regulatory authority guidelines and requirements
- Maintaining collaborative, proactive, and effective communication with both client and internal teams
Must meet the following requirements for consideration:
- Bachelor's degree (minimum)
- 10+ years of regulatory writing experience with clinical- related documentation
- Knowledge of global health authority requirements
- Strong understanding of the document creation process and of the drug development lifecycle
- Intermediate proficiency with Microsoft Word skills
- Ability to communicate difficult and complex ideas clearly and effectively to all stakeholders
