FDA & Regulatory Compliance Attorney
Quick facts
- Type
- Part-time
- Location
- Remote
- Background
- JD / attorney
- Experience
- 5+ years
- Platform
- Micro1 — 259 open jobs
- Typical pay at Micro1
- $20–120/hour · median $90 (22 jobs on our site)
- Apply
- Free to apply — never pay to get AI training work
pay
Required Skills
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
About micro1
micro1 is a data lab that helps AI labs & Enterprises train foundational models and agents. We provide frontier evaluations and reinforcement learning environments to improve LLM capabilities, as well as contextual evaluations to monitor and improve AI agents in enterprise settings.
Our AI recruiting agent sources and vets domain experts for our data platform that enables rapid production of high-quality training data. Our research spans high-value, specialized domains (legal, medical, finance, coding, etc.), where expert-level data is the hardest to produce and most valuable for advanced model performance. Our pipeline performance system ensures both quality and velocity.
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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micro1 recruits engineers and domain experts for AI labs using its AI interviewer. Once vetted, contractors work on human-data projects such as writing and checking model outputs or building coding evaluations.