Offer summary
Qualifications:
Bachelor of Science in a related field required, 8+ years in pharma industry required, 5+ years in regulatory writing for Medical Writer, Strong understanding of drug development and regulations, Experience in writing clinical documents needed.
Key responsabilities:
- Lead the compilation and editing of clinical documents
- Interpret data and analyze published literature
- Collaborate with cross-functional teams professionally
- Develop relevant SOPs, templates, and manuals
- Project manage work of contract medical writers