Offer summary
Qualifications:
Bachelor's degree in scientific discipline, 2-5 years of relevant writing experience, Experience in pharmaceutical/CRO industry preferred, Advanced medical writing qualifications advantageous, In-depth knowledge of regulatory guidelines.
Key responsabilities:
- Research, write, and edit regulatory documents
- Manage medical writing projects independently
- Develop project timelines, standards, and budgets
- Represent department as primary project contact
- Assist with business development activities