Edison Scientific
Regulatory Affairs
$180K–$250K
San Francisco +2 · On-site · Full-time · Posted Oct 16, 2026
- Location
- San Francisco
New York
Boston - Experience
- 5+ years; sponsor organization experience is stated as ideal.
- Education
- Bachelor's degree required; advanced degree preferred (Ph.D., Pharm.D., M.D., or M.S. in a life sciences discipline).
About the job
Evaluates and improves AI-generated regulatory and medical writing, partnering onsite with life sciences clients to deploy agents and ensure submission-ready documents.
What you'll do
- Evaluate AI-drafted regulatory content for scientific accuracy, guideline compliance, consistency, and narrative quality; improve agent performance.
- Develop benchmarks and acceptance criteria, and validate AI-generated documents with partner teams.
- Deploy AI agents into partner workflows and collaborate with engineers and go-to-market teams on implementation and evaluation.
What they ask for
- 5+ years of Regulatory Affairs or Medical Writing experience in the pharmaceutical or biotechnology industry.
- Bachelor's degree.
- Strong understanding of regulatory requirements, including ICH guidelines and FDA/EMA expectations.
- Hands-on regulatory document authoring experience and familiarity with eCTD structure and the end-to-end submission process.
Nice to have
- Advanced degree in a life sciences discipline (Ph.D., Pharm.D., M.D., or M.S.); experience in listed therapeutic areas.
- Familiarity with AI-assisted writing or document automation tools.
Pay
USD $180,000 - $250,000 • Offers equity (salary); USD $180K – $250K • Offers Equity (compensation)
Tools
AI scientist agents, Veeva Vault, Documentum, ICH guidelines, FDA, EMA, eCTD
AI focus
Evaluates and improves AI agents for regulatory and medical writing, builds quality benchmarks, and helps integrate AI-generated documents into submission workflows.
Model-written summary · the original posting is authoritative