AI training contract
FDA & Regulatory Compliance Attorney
Legal · USD 140-400 an hour. · 5 openings
FDA & Regulatory Compliance Attorney is contract work for micro1, reviewing and correcting what AI models produce in legal. 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. This role is gated on bar admission. Applications without it are not considered, and the requirement is stated here because the original advert usually carries it well below the rate.
What it pays. USD 140 to USD 400 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, Yemen, and Ethiopia. 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 5 openings on this role.
Skills named: fda regulatory analysis, legal research, regulatory compliance, risk assessment, regulatory submissions, legal writing, verbal communication, life sciences industry knowledge, attention to detail, issue spotting and resolution.
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: FDA & Regulatory Compliance Attorney Role Type: Contractor Location: Remote micro1 is engaging FDA & Regulatory Compliance Attorneys to collaborate on a project supporting regulatory and legal compliance initiatives for a valued customer. 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 Analyze and interpret FDA statutes, regulations, and guidance documents to provide domain-specific insights. Review and critique regulatory submissions, compliance documentation, and procedural materials. Assess real-world scenarios for regulatory risk, enforcement trends, and liability considerations. Draft or edit scenario-based questions and answers elucidating regulatory best practices. Identify emerging issues in FDA and broader regulatory compliance and recommend practical solutions. Generate clear, concise written and verbal explanations of complex legal requirements for technical and non-technical audiences. Contribute to the continuous improvement of project deliverables through feedback on content accuracy and completeness. Preferred Qualifications Juris Doctor (JD) degree and active license to practice law in the United States. 5+ years of experience focused on FDA law, regulatory strategy, or compliance in life sciences, pharmaceuticals, or medical devices. Strong understanding of federal regulatory processes, submission pathways, and compliance protocols. Outstanding written and verbal communication skills, with proven ability to convey complex legal concepts clearly. Experience advising or representing clients in FDA investigations, warning letters, or consent decrees is advantageous. Ability to navigate ambiguity and distill actionable insights from regulatory developments. Detail-oriented approach and commitment to producing high-quality, accurate content.
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Rate, openings and requirements checked 2026-10-22 against micro1's own public postings.