Are you a seasoned medical writer ready to shape the future of drug development? Join a hyper-growth startup revolutionizing regulatory document authoring with cutting-edge AI. You’ll work directly on products impacting thousands of professionals at leading pharma organizations.
What You’ll Do:
- Design and evaluate AI systems for regulatory writing
- Bridge medical writing expertise with technical product development
- Ensure quality control and identify edge cases in AI-generated content
What We’re Looking For:
- 3+ years in medical writing (regulatory affairs)
- Experience with CTD documents (non-clinical & CMC)
- Knowledge of FDA, EMA, ICH guidelines
- Strong QC skills and ability to translate rules for technical teams
Bonus Points:
- Familiarity with XML/JSON formats
- Experience with life sciences software tools
Why Apply?
- Competitive salary ($110K–$120K) + equity
- Hybrid work model (4–5 days onsite, Mon–Sat)
- Direct impact, rapid career growth, and exposure to top-tier pharma clients
- High-intensity, innovative startup culture
Ready to accelerate your career and make a real difference? Apply now to learn more!
Job Type: Full Time
Job Locations: Usa