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Disease-Area Clinician — Trial Endpoints & Prescribing

Mercor · 100% remote · Contract · Posted

Pay
$150–230/hr
Location
United States
Languages
English
Hours
10-20 hours over 1-2 week pilot
Openings
Not listed
Level
Expert
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Summary

Create and critique rubrics analyzing commercial drugs and drug-development programs, interpret clinical trial endpoints, and judge whether results would change prescribing for a set of drugs in a specific therapeutic area.

What you'll do

  • Create and critique rubrics analyzing commercial drugs and drug-development programs
  • Interpret clinical trial endpoints and judge whether results would change prescribing
  • Assess real-world uptake implications in the therapeutic area
  • Apply across the pilot's set of drugs and programs

Requirements

  • Be a US-based disease-area clinician (practising physician, MD/DO)
  • Be familiar with biotech/pharma development programs
  • Have deep expertise in a specific therapeutic area
  • Be board-certified and actively practising in the specialty

Skills

  • Clinical Trial Endpoints
  • Drug Development Programs
  • Therapeutic Area Expertise
  • Prescribing Practices

Full description

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

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