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FDA & Regulatory Compliance Attorney

$400
per hour
Contractor Remote Last verified 21 Jul 2026
Affiliate disclosure

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About the Role

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.

What You'll Do

  • 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.

You're a Good Fit If You

  • 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
  • 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.

Role Highlights

Pay
$140-$400/h
Contract
Contractor
Location
Remote
Category
Model evaluation
Posted
10 days ago
Job ID

Pay & Payout

Engaged directly through micro1. Apply via the link below - micro1 handles onboarding and payment.

Common Questions

micro1 has a reliability rating of reliable based on the listings we track, with an onboarding time of 1-3 days. See our full micro1 review for the details behind that rating.

Applying takes you to micro1's own website, where the application is completed. We are not a recruiter or employer and do not process applications directly - we may be recorded as the referring source.

$140-$400/h - Engaged directly through micro1. Apply via the link below - micro1 handles onboarding and payment.

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.

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About micro1 for this role

We track 368 open micro1 roles on AI Work Expert. Across 535 hourly listings, the typical micro1 rate runs from $50 to $90 an hour; this role lists $140-$400/h. Our reliability rating for micro1 is reliable, with an onboarding time of 1-3 days.