Description review
Regulatory Affairs Consultant - Fully Remote | Upto $170/hr
mercor · United States · back to the listing
HR standards
70/100
solid
Title ↔ description
49/100
poor
Reads as
Unclear
no confident match
What the listing never says
- No pay range published. Candidates cannot tell whether applying is worth their time. Pay transparency
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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 years1 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 years1 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