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Law · Remote · via micro1High demand

FDA & Regulatory Compliance Attorney

$140–$400/hr

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.

Skills they want

  • 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

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