Role Description
We are sharing a specialised remote consulting opportunity for experienced FDA & Regulatory Compliance Attorneys with deep expertise in US food and drug law, life sciences regulation, regulatory strategy, and compliance to contribute their professional knowledge to advanced AI training and evaluation initiatives.
Selected professionals will:
-
Analyse FDA statutes and regulatory guidance.
-
Review compliance documentation.
-
Develop realistic legal scenarios.
-
Evaluate AI-generated regulatory content.
The work combines legal research, regulatory risk assessment, technical document analysis, and subject-matter evaluation to help improve the accuracy, reasoning, and reliability of AI systems operating across pharmaceuticals, medical devices, and regulated life sciences environments. Prior AI experience is not required.
Qualifications
-
Juris Doctor (JD) degree and active licence to practise law in the United States.
-
At least 5 years of professional experience focused on FDA law, regulatory compliance, or regulatory strategy.
-
Strong legal expertise within the pharmaceutical, medical device, biotechnology, or broader life sciences industries.
-
Comprehensive understanding of FDA statutes, federal regulations, regulatory guidance, and administrative processes.
-
Practical knowledge of regulatory submission pathways, compliance protocols, and agency expectations.
-
Demonstrated experience reviewing regulatory documentation, interpreting legal requirements, and conducting detailed legal research.
-
Strong ability to identify regulatory risks, compliance deficiencies, and potential liability considerations.
-
Experience advising or representing clients in FDA investigations, warning letter responses, or consent decree matters is advantageous.
-
Familiarity with emerging regulatory developments and evolving compliance expectations across regulated life sciences sectors.
-
Excellent legal writing, analytical reasoning, problem-solving, and attention-to-detail skills.
-
Ability to interpret complex or ambiguous regulatory requirements and translate findings into clear, actionable explanations.
-
Outstanding written and verbal communication skills, including experience communicating with legal, regulatory, and technical stakeholders.
-
Ability to work independently and contribute effectively to remote, collaborative research assignments.
-
Prior experience with AI training, model evaluation, or regulatory technology applications is not required.
Requirements
-
Freelance / contract engagement.
-
Fully remote.
-
Compensation: $140β$400/hour.
-
5 available openings.
-
Specialised legal consulting role spanning FDA law, regulatory compliance, life sciences regulation, and AI training.
-
Work will involve regulatory research, legal document review, scenario development, risk assessment, and AI-generated content evaluation.
-
Assignments will draw on practical legal expertise in federal regulatory processes, compliance obligations, enforcement considerations, and regulatory submissions.
-
Collaboration will take place remotely through designated project communication and workflow tools.
-
Prior experience working with AI systems is not required.
-
Work must be completed without using confidential or proprietary information belonging to any employer, client, institution, or other third party.
Company Description
This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.
By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy:
https://www.24-mag.com/privacy-policy