Job Summary
A research services company is seeking a Remote Associate Medical Writer.
Individual must be able to fulfill the following responsibilities:
- Write, edit, and review Essential Documents
- Perform quality control (QC) reviews
- Write, edit, review, finalize, and track CSR safety narratives
Position Requirements Include:
- 2 years of corresponding industry experience working with clinical documentation and data
- Relevant educational background or equivalent education, training, and experience
- Prior pharmaceutical, biotechnology, or contract research organization experience
- Basic knowledge of global regulations and guidelines on drug the development process
- Basic knowledge of electronic Common Technical Document (eCTD) requirements
- Intermediate proficiency in MS Office
