Job Summary
A global research company is in need of a Telecommute Scientific Regulatory Writer.
Individual must be able to fulfill the following responsibilities:
- Write clinical documents for submission to US and global regulatory authorities
- Serve as the medical writer on assigned projects
- Ensure documents are produced in accordance with procedures
Must meet the following requirements for consideration:
- Previous experience writing regulatory reports and related documents
- Strong command of medical and surgical terminology
- Demonstrated ability to identify and adapt to shifting priorities and competing demands
- Proficiency in document development and management using Word, Excel, PowerPoint and EndNote
- Training and degree in science, engineering, or medical fields
- Scientific research background