Offer summary
Qualifications:
Bachelor's degree in Life Science or English/Communications, 6+ years of medical writing experience, Knowledge of FDA regulations and ICH guidelines, Experience with regulatory submissions (CTA/IND/NDA/BLA), Proficiency in Microsoft Office Suite.
Key responsabilities:
- Produce high quality clinical documents
- Independently write and edit key documents
- Manage review and finalization processes
- Collaborate across various project teams
- Contribute to SOP and template development