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Open nowPosted 48 days ago

Disease-Area Clinician - Trial Endpoints & Prescribing

Workable (global search)108,016 open roles

Where
United States
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Remote
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Your applicationOpen nowDisease-Area Clinician - Trial Endpoints & PrescribingWorkable (global search) · United States
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  5. 34.0%30 days
This job: posted 48 days ago

Workable (global search) median: 7 days open

The posting

This role is for one of our clients

Compensation: $150 - $230 per hour

We are seeking experienced US-based practicing physicians to contribute to an expert evaluation project focused on assessing commercial drugs and drug-development programs.

As a Disease-Area Clinician, you will apply your clinical expertise to evaluate clinical trial evidence, interpret endpoints, and assess whether study results are likely to influence prescribing decisions and real-world adoption within your therapeutic area.

This opportunity is designed for board-certified physicians with deep expertise in a specific disease area and familiarity with pharmaceutical and biotechnology development programs.

Requirements

Key Responsibilities

  • Develop and critically review evaluation rubrics for commercial drugs and drug-development programs.
  • Interpret clinical trial endpoints, study results, and efficacy/safety data within your area of specialty.
  • Assess whether clinical trial findings are meaningful from a practicing physician's perspective.
  • Evaluate whether trial outcomes are likely to influence prescribing decisions and clinical practice.
  • Assess the potential impact of clinical evidence on real-world treatment adoption and utilization.
  • Apply disease-area expertise to evaluate multiple drugs and development programs within the assigned therapeutic area.
  • Provide clear, evidence-based reasoning behind clinical assessments and recommendations.
  • Collaborate with other subject-matter experts to ensure evaluations are clinically rigorous, consistent, and grounded in current medical practice.

Requirements

  • MD or DO with active clinical practice in the United States.
  • Board certification in a relevant medical specialty.
  • Active, unrestricted medical licensure in the United States.
  • Deep clinical expertise in a specific therapeutic or disease area.
  • Current or recent hands-on clinical practice within the relevant specialty.
  • Familiarity with biotechnology and pharmaceutical drug-development programs.
  • Strong understanding of clinical trials, endpoints, treatment outcomes, and evidence-based prescribing.
  • Ability to translate complex clinical evidence into clear, structured written reasoning.
  • Strong attention to detail and sound clinical judgment.

Engagement Details

  • Role: Disease-Area Clinician — Trial Endpoints & Prescribing
  • Engagement: Paid pilot
  • Duration: Approximately 10–20 hours over a 1–2 week period
  • Location: Fully Remote
  • Eligibility: US-based physicians
  • Potential: Strong contributors may have opportunities for recurring engagements as the program expands.

Why Participate?

  • Apply your clinical expertise to help improve how AI systems evaluate pharmaceutical and clinical evidence.
  • Contribute to more accurate, expert-level AI evaluation of drugs and drug-development programs.
  • Work on a flexible, focused research engagement.
  • Potential for continued opportunities based on project needs and performance.

Contract and Payment Terms

  • You will be engaged as an independent contractor.
  • This is a fully remote opportunity with flexible scheduling.
  • Projects may be extended, shortened, or concluded early depending on project requirements and performance.
  • The engagement will not require access to confidential or proprietary information belonging to any employer, client, or institution.
  • Payments are made weekly based on services rendered through available payment platforms.
  • H-1B and STEM OPT candidates are not currently supported.

Equal Opportunity

We consider all qualified applicants without regard to legally protected characteristics and provide reasonable accommodations upon request.

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