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