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