Regulatory Affairs Consultant - Fully Remote | Upto $170/hr

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) • Upload resume • AI interview based on your resume • Submit form Resources & Support • For details about the interview process and platform information, please check: • For any help or support, reach out to: PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity. Originally posted on Himalayas