What the work is
You write and grade evaluation tasks built on clinical study reports and safety reports, checking whether AI drafts follow ICH structure and stay faithful to the source tables. Each judgement needs a clear written reason.
Who gets hired
- 5+ years of regulatory medical writing at a sponsor, CRO or as a consultant
- Has authored full Clinical Study Reports
- Fluent in ICH E3, E2F, E2C and eCTD
- Advanced life-science degree or equivalent authoring depth; oncology/haematology valued
Pay
$30–60/hr, fully remote. How payouts and tax work.