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Hiring now · posted today Law Contract · Remote

FDA & Regulatory Compliance Attorney

$140–$400/hr

Published pay. The final rate depends on your test, experience and country.

Remote · Worldwide 5 openings Language: English Posted 22 Oct 2026

About this role

Role Title: FDA & Regulatory Compliance Attorney

Role Type: Contractor

Location: Remote

our partner 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.

This is a 100% remote contract role, open to applicants worldwide in the countries the employer accepts.

fda regulatory analysislegal researchregulatory compliancerisk assessmentregulatory submissionslegal writingverbal communicationlife sciences industry knowledgeattention to detailissue spotting and resolution

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What to know before you apply

Pay
At the published rate, 10 hours a week would be about $1,400–$4,000 and 20 hours about $2,800–$8,000 before tax. Hours depend on the project, so treat this as a ceiling, not a promise.
Location
Open worldwide in the countries the employer accepts. Payments usually go out through services like PayPal or Wise, so check one of them works in your country.
Credentials
The listing asks for a law degree / bar admission, 5+ years of experience. Put it in the first line of your profile: reviewers screen for it before anything else.
Timing
This listing is new today. Projects can close once they have enough people, so it is worth applying while it is open.
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