Job Summary
A staffing agency has an open position for a Remote Senior Rare Disease Biopharma Clinical and Regulatory Writing Manager.
Core Responsibilities of this position include:
- Ensuring document management from start to finish
- Overseeing and editing documents
- Serving as lead for document review
Applicants must meet the following qualifications:
- 2-5 years in biotech/pharma industry
- Experience within medical writing including editing and clinical development
- Experience authoring CSRs, IBs, protocols, and safety reports
- Leadership experience and project management skills
