AI training contract
Regulatory Affairs Specialist
Medicine & Health · USD 50-80 an hour. · 30 openings
Regulatory Affairs Specialist is contract work for micro1, reviewing and correcting what AI models produce in medicine & health. The output of the job is expert judgement written down: a model gives an answer, someone who knows the subject decides whether it is right and explains why.
What it requires. No credential is stated on this listing beyond experience in the field.
What it pays. USD 50 to USD 80 an hour, as published by micro1. Rates in this category track how rare the credential is rather than how hard the work is.
Where. The listing says this role is remote and names no country. micro1 says it hires talent from around the world, except people who reside in Afghanistan, Belarus, China, Cuba, Democratic Republic of the Congo, Hong Kong, Iran, Iraq, Libya, Macao, Myanmar, North Korea, Russian Federation, Somalia, South Sudan, Sudan, Syria, Venezuela, Ukraine, and Yemen. So this page lists every other country as eligible, on the strength of that rule and not of anything this listing says. Requirements can still differ by role, so check the application page on micro1 before you apply.
micro1 lists 30 openings on this role.
Skills named: regulatory affairs, clinical documentation review, ich guidelines, ctd/ectd structure, written communication, critical thinking, regulatory submissions, health authority interactions, attention to detail, remote collaboration.
Applications are made on micro1, not here. WFA Digital is independent of micro1 and may receive a referral fee if you are hired, at no cost to you.
Full listing, as published by micro1
Role Title: Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. Scope of Work Author and review evaluation tasks inspired by real-world agency requests and sponsor response threads, determining if drafted responses meet regulatory expectations. Apply expert judgment to review clinical documentation, assessing whether conclusions are substantiated, commitments are properly scoped, and records can withstand regulatory scrutiny. Distinguish between substantively adequate and superficially polished responses, articulating clear rationales for any deficiencies. Assess consistency across comprehensive document sets, identifying unsupported or conflicting claims within or between documents. Provide structured, well-reasoned written feedback grounded in applicable regulatory guidelines rather than subjective impressions. Collaborate asynchronously and communicate complex regulatory concepts clearly in both written and verbal form. Preferred Qualifications 5+ years of direct regulatory affairs experience at a sponsor, CRO, or consultancy, with responsibility for clinical submissions. Documented experience drafting or leading responses to health authority information requests, particularly for ongoing regulatory filings. Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). Proven ability to critically read clinical or safety documents to identify regulatory risks, unsupported statements, and potential reviewer concerns. Exceptional written communication skills, with the capability to convey regulatory reasoning clearly, concisely, and defensibly. Degree in life sciences, pharmacy, medicine, or a related field; RAC certification is an advantage. Experience engaging with multiple regions or agencies, prior health authority reviewer/assessor background, or familiarity with AI-assisted regulatory tools (all considered valuable).
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Rate, openings and requirements checked 2026-09-25 against micro1's own public postings.