Healthcare & FDA Regulatory Law Expert

What You'll Do5

• Evaluate AI-generated responses to hypothetical U.S. healthcare law questions covering HIPAA privacy and security rules, Anti-Kickback Statute safe harbors, Stark Law exceptions, and FDA approval pathways like 510(k), PMA, and NDA.
• Apply a detailed legal rubric to check issue spotting, regulatory accuracy, and correct use of CMS guidance and FDA rules.
• Spot logical gaps in AI reasoning about fraud and abuse compliance, clinical trial regulations, telehealth law, and pharmacy benefit management.
• Write clear, thorough annotations and feedback that help refine AI model behavior.
• Work with researchers and project managers to keep evaluation standards consistent and aligned with project goals.

Requirements5

• Juris Doctor (J.D.) from an accredited U.S. law school and active or inactive bar admission.
• At least 3 years of U.S. legal practice focused on healthcare law, FDA regulatory affairs, or healthcare compliance.
• Solid grasp of HIPAA, the Anti-Kickback Statute, Stark Law, the False Claims Act, and FDA regulations.
• Strong analytical writing and close attention to detail.
• High ethical standards and a genuine interest in AI applications for law.

Preferred Qualifications1

• Interest in AI and its use in the legal field

Who Should Apply

Candidates with a J.D., active or inactive bar membership, and 3+ years in U.S. healthcare law or FDA regulatory work will thrive here. The role suits attorneys who enjoy dissecting Stark Law exceptions, False Claims Act liability, and pre-market approval pathways while contributing to AI model quality.

Salary Insight