About the job
Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.
Position: Clinical Regulatory Expert Type:Contract Compensation:$130–$170/hour Location:Remote Commitment:20–25 hours/week
Role Responsibilities
Validate clinical data rooms and documents against FDA evidentiary standards and formatting expectations.
Author FDA information requests and model responses. Design prompts, golden outputs, and rubrics to quantify AI agent capabilities.
Ensure compliance with deliberate defects testing regulatory judgment.
Work independently and asynchronously to meet deadlines and improve AI model performance.
Qualifications
Must-Have
5+ years of experience in regulatory roles.
MD, PhD, PharmD, or equivalent.
Experience reviewing or responding to FDA information requests across CMC, patient-level data, investigator qualifications, and biomarker or endpoint evidence.
No conflict of interest with a current federal employer.
Preferred
10–25 years of experience.
Direct FDA review experience preferred over sponsor-side liaison work.
Application Process (Takes 20–30 mins to complete)
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Mercor connects elite creative and technical talent with leading AI research labs. The company specializes in matching top-tier professionals with AI research organizations to support advanced projects. Mercor facilitates work across multiple domains including financial analysis, hedge fund strategy evaluation, and deal structuring, leveraging AI to enhance model training and research capabilities. The company bridges the gap between specialized talent and cutting-edge AI research institutions.
