Regulatory Affairs Consultant - Fully Remote | Upto $170/hr
Budget / Salary$130–170
TypeContract
LocationUnited States
Posted2 hours ago
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
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
Apply on Himalayas →
Job sourced from Himalayas. Applications happen directly on the original platform — we never collect your data.