Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowFirst seen 4 days ago

Remote | FDA & Regulatory Compliance Attorney — $140–$400/hour

24-MAG343 open roles

Where
New York, United States, Remote
Work mode
Remote
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowRemote | FDA & Regulatory Compliance Attorney — $140–$400/hour24-MAG · New York, United States, Remote

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on 24-MAG's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. 24-MAG postings stay open a median of 1 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.7%14 days
  5. 35.6%30 days
  6. 58.0%60 days
This job: first seen 4 days ago

24-MAG median: 1 days open

The posting

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, and 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.

Key Responsibilities

FDA Regulatory Research & Legal Analysis

  • Analyse and interpret FDA statutes, federal regulations, guidance documents, and relevant administrative requirements
  • Conduct detailed legal research across pharmaceutical, medical device, and broader life sciences regulatory frameworks
  • Evaluate regulatory requirements affecting product development, approval pathways, marketing, and ongoing compliance
  • Examine FDA regulatory interpretations and their implications for regulated organisations and industry practices
  • Apply professional legal judgement to complex regulatory questions involving statutory interpretation and agency guidance

Regulatory Submissions & Compliance Documentation

  • Review and assess FDA regulatory submissions, compliance documentation, and procedural materials
  • Evaluate documentation for accuracy, completeness, regulatory consistency, and alignment with applicable requirements
  • Analyse regulatory submission pathways and associated legal obligations across relevant product categories
  • Identify documentation issues, regulatory inconsistencies, and areas requiring additional legal or technical clarification
  • Provide detailed commentary on regulatory processes, compliance protocols, and documentation quality

Regulatory Risk Assessment & Enforcement Analysis

  • Assess realistic legal scenarios involving FDA compliance risks, enforcement trends, and potential liability considerations
  • Analyse regulatory issues associated with inspections, investigations, enforcement actions, and compliance deficiencies
  • Evaluate legal considerations relating to FDA warning letters, corrective actions, and regulatory remediation
  • Identify emerging regulatory developments and their implications for life sciences organisations
  • Apply risk assessment and issue-spotting expertise to recommend practical, legally grounded approaches to regulatory challenges

AI Training & Regulatory Content Evaluation

  • Develop realistic legal questions, scenario-based exercises, and case studies reflecting FDA regulatory practice
  • Review, edit, and validate AI-generated explanations, regulatory analyses, and compliance-related responses
  • Identify legal inaccuracies, incomplete regulatory reasoning, and areas requiring greater technical or procedural precision
  • Translate complex FDA requirements into clear, structured content suitable for specialised AI training and evaluation
  • Provide constructive written feedback to strengthen the accuracy, completeness, and professional relevance of AI-generated regulatory materials

Legal Quality Assurance & Research Collaboration

  • Produce clear regulatory analyses, legal research summaries, scenario assessments, and structured evaluation feedback
  • Apply rigorous quality standards to materials involving FDA requirements, regulatory submissions, and compliance obligations
  • Communicate complex legal and regulatory concepts effectively to technical and non-technical audiences
  • Collaborate remotely with project stakeholders and other contributors on specialised regulatory research assignments
  • Support the continuous improvement of research methodologies, content accuracy, and overall project deliverable quality

Ideal Profile

  • 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

Engagement Details

  • Freelance / contract engagement
  • Fully remote
  • Compensation: $140–$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

About the Platform

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

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against 24-MAG's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on 24-MAG's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    24-MAG's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.