Offer summary
Qualifications:
6+ years of regulatory medical writing experience, Bachelors/advanced degree in life sciences or healthcare, Experience authoring clinical documents, Knowledge in multiple therapeutic areas, Experience from the pharmaceutical/CRO industry.
Key responsabilities:
- Research, create, and edit clinical research documents
- Act as project lead writer and coordinator
- Manage contributions of multiple writers
- Facilitate process improvement and training
- Support sales process with client liaison and proposals