Disease-Area Clinician, Trial Endpoints & Prescribing
$150 to $230/hIndicative range provided by Mercor
Posted on August 5, 2026 · Applications until December 3, 2026
Only: United States
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This remote role involves creating and critiquing rubrics that analyze commercial drugs and drug development programs while interpreting clinical trial endpoints. Candidates must be US based board certified and actively practicing physicians with deep expertise in a specific therapeutic area.
Description in English, as published by Mercor.
Mercor is partnering with a biotech and pharma research team on expert human-evaluation work, creating and critiquing rubrics that analyze commercial drugs and drug-development programs. We're seeking a disease-area clinician for a paid pilot, with the potential to continue as the work scales.
Responsibilities
- Create and critique rubrics that analyze commercial drugs and drug-development programs
- Interpret clinical trial endpoints and judge whether results would change prescribing
- Assess what that means for real-world uptake in your therapeutic area
- Apply this across the pilot's set of drugs and programs
Requirements
- US-based disease-area clinician (practising physician, MD/DO)
- Familiarity with biotech/pharma development programs
- Deep expertise in a specific therapeutic area
- Board-certified and actively practising in your specialty
Engagement Details
- Duration: Approximately 10, 20 hours over a 1, 2 week pilot
- Remote, US-based
Why Participate
- Help improve expert AI evaluation of drugs and drug-development programs
- Recurring engagement for strong contributors
5 openings
Only: United States
About Mercor
Mercor is a US marketplace hiring remote experts for AI and consulting projects, from law to engineering. The original posting is on their site.
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