FDA & Regulatory Compliance Attorney
micro1Legit · not rated yetPosted 4 days ago
Pay: $140–400/hr
- Who can apply
- Countries not stated in the listing
- Hours
- Hours vary · Freelance
- Where
- Remote, work from home
- Job type
- Expert (SME) review
- Openings
- 5 openings
At a glance: A freelance, remote expert (SME) review job with micro1. It pays $140–400/hr, with hours that vary. The listing doesn't say which countries can apply.
Countries not stated
The posting doesn't say which countries can apply, so check before you apply. What micro1 says in general: Recruits worldwide apart from residents of 21 countries and regions, among them China, Russia, Ukraine, Iran, Venezuela and Ethiopia; some listings accept applicants from the US, UK or Canada only
We may earn a referral fee if you are hired. How we make money
What happens after you click Apply
- You leave AI Trainer HQ and go to micro1’s own site.
- Pick a role, apply and answer the screening questions attached to it
- Sit the AI interview with Zara, spoken and recorded, about 20–40 minutes
- Complete a technical assessment if the role has one, then a hiring-manager review
- Take the offer, sign your Deel contract and clear the KYC identity check
How this pay compares
This job pays more than 84% of the 86 other law jobs on the board that state pay; 0% pay more.
- This job
- $270/hrMiddle of $140–400/hr
- Median on micro1
- $65/hrFrom 287 other paid jobs
- Median in law
- $113/hrFrom 86 other paid jobs
Requirements
- Qualifications
- Fda regulatory analysis
- Legal research
- Regulatory compliance
- Risk assessment
- Regulatory submissions
- Legal writing
- Verbal communication
- Life sciences industry knowledge
- Languages
- English
- Equipment
- Computer with a reliable internet connection
About this job
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.
Listing history
- First seen on our board
- (4 days ago)
- Posted by micro1
- (4 days ago)
- Last checked
- Source
- micro1
We check every live job against its source at least every 24 hours. How we check jobs
