Job Summary
A staffing firm needs applicants for an opening for a Remote Global Biopharma Principal Medical Writer in Chicago.
Candidates will be responsible for the following:
- Planning and coordinating the review, approval, QC, and more of the production of regulatory projects
- Presenting leadership as well as project management for compound programs
- Preparing documents of high-quality that are founded in regulation and supported by science
Qualifications for this position include:
- BS in Science with significant relevant writing experience or BS in English with significant relevant science experience
- At least 4 years of experience within medical/regulatory writing
- At least 2 years of management experience