FDA Regulatory Compliance Attorney (English)

OpenTrain AI, Inc.; USA; Remote; USD 193.000 - 551.000; Teilzeit

Zusammenfassung

OpenTrain AI, Inc. is seeking an FDA Regulatory Compliance Attorney (English) to provide legal analysis for AI training projects focused on FDA regulatory compliance. The role requires a U.S.

law license and at least five years of FDA experience, with compensation ranging from $140 to $400 per hour in a remote, part-time capacity. The candidate will review statutes, regulations, submissions, and compliance materials, assess regulatory risk, and draft scenario-based questions and guidance for

Qualifikationen

• Must have fluent English.
• Active license to practice law in the United States.
• At least five years in FDA law, regulatory strategy, or compliance.
• Background in life sciences, pharmaceuticals, or medical devices.

Aufgaben

• Provide legal analysis for FDA regulatory compliance in AI training projects.
• Review and critique FDA statutes, regulations, and guidance documents.
• Assess regulatory risk, enforcement trends, and liability issues.
• Draft or edit scenario-based questions and answers about regulatory best practices.
• Identify emerging FDA and broader compliance issues and recommend practical solutions.
• Explain complex regulatory requirements to technical and non-technical audiences.
• Provide feedback to improve accuracy and completeness of deliverables.

Kenntnisse

FDA regulatory analysis

Regulatory strategy

Legal writing

Regulatory compliance

Jobbeschreibung

FDA Regulatory Compliance Attorney (English)

Review FDA statutes, regulations, submissions, and compliance materials while helping create reliable legal examples for AI training. This contract, part-time role pays $140 to $400 per hour and requires a U.S. law license plus five years of FDA experience.

Remote Hourly · $140–$400/hr

$140–$400/hr

Compensation

Contract, part-time

Engagement

Remote

Location

Oct 22, 2026

Posted

Open in 52 countries

United States + more

• Algeria
• Argentina
• Austria
• Bahrain
• Bangladesh
• Belgium
• Brazil
• Canada
• Chile
• Colombia
• Denmark
• Egypt
• France
• Germany
• Ghana
• Greece
• India
• Indonesia
• Italy
• Japan
• Jordan
• Kazakhstan
• Kenya
• Kuwait
• Kyrgyzstan
• Lebanon
• Malaysia
• Mexico
• Morocco
• Netherlands
• Nigeria
• Oman
• Pakistan
• Palestine
• Peru
• Philippines
• Portugal
• Qatar
• Saudi Arabia
• Singapore
• South Africa
• Spain
• Sri Lanka
• Switzerland
• Taiwan
• Thailand
• Tunisia
• United Arab Emirates
• United Kingdom
• United States
• Uzbekistan
• Vietnam

The work

You will provide legal analysis for AI training projects focused on FDA regulatory compliance. The work involves turning specialized FDA and life sciences knowledge into clear, accurate examples of legal reasoning and regulatory best practices.

• Analyze FDA statutes, regulations, and guidance documents.
• Review and critique regulatory submissions, compliance documents, and procedures.
• Assess regulatory risk, enforcement trends, and liability issues.
• Draft or edit scenario-based questions and answers about regulatory best practices.
• Identify emerging FDA and broader compliance issues and recommend practical solutions.
• Explain complex legal requirements to technical and non-technical audiences.
• Give feedback to improve the accuracy and completeness of project deliverables.

What it pays and takes

This is a contract, part-time role. The work is open to candidates in the countries listed for the role, including the United States, Canada, the United Kingdom, India, Singapore, and other locations across the listed regions.

• Pay: $140 to $400 per hour.
• Language: Fluent English is required.
• License: Active license to practice law in the United States required.
• Experience: At least five years in FDA law, regulatory strategy, or compliance.
• Background: Experience in life sciences, pharmaceuticals, or medical devices.
• Knowledge: Strong understanding of federal regulatory processes, submission pathways, and compliance protocols.
• Skills: Excellent written and verbal communication, careful judgment, attention to detail, and the ability to turn complex developments into practical guidance.
• Helpful background: Advising or representing clients in FDA investigations, warning letters, or consent decrees.

About AI training work

AI training is the human work behind systems that learn from examples. Legal experts help by reviewing information, writing and rating responses, and creating accurate examples so AI systems handle specialized questions more reliably.

Requirements

• Experience: Entry level