Role Description
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.
Key Responsibilities
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Develop and critically review evaluation rubrics for commercial drugs and drug-development programs.
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Interpret clinical trial endpoints, study results, and efficacy/safety data within your area of specialty.
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Assess whether clinical trial findings are meaningful from a practicing physician's perspective.
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Evaluate whether trial outcomes are likely to influence prescribing decisions and clinical practice.
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Assess the potential impact of clinical evidence on real-world treatment adoption and utilization.
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Apply disease-area expertise to evaluate multiple drugs and development programs within the assigned therapeutic area.
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Provide clear, evidence-based reasoning behind clinical assessments and recommendations.
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Collaborate with other subject-matter experts to ensure evaluations are clinically rigorous, consistent, and grounded in current medical practice.
Requirements
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MD or DO with active clinical practice in the United States.
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Board certification in a relevant medical specialty.
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Active, unrestricted medical licensure in the United States.
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Deep clinical expertise in a specific therapeutic or disease area.
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Current or recent hands-on clinical practice within the relevant specialty.
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Familiarity with biotechnology and pharmaceutical drug-development programs.
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Strong understanding of clinical trials, endpoints, treatment outcomes, and evidence-based prescribing.
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Ability to translate complex clinical evidence into clear, structured written reasoning.
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Strong attention to detail and sound clinical judgment.
Engagement Details
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Role: Disease-Area Clinician β Trial Endpoints & Prescribing
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Engagement: Paid pilot
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Duration: Approximately 10β20 hours over a 1β2 week period
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Location: Fully Remote
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Eligibility: US-based physicians
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Potential: Strong contributors may have opportunities for recurring engagements as the program expands.
Why Participate?
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Apply your clinical expertise to help improve how AI systems evaluate pharmaceutical and clinical evidence.
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Contribute to more accurate, expert-level AI evaluation of drugs and drug-development programs.
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Work on a flexible, focused research engagement.
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Potential for continued opportunities based on project needs and performance.
Contract and Payment Terms
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You will be engaged as an independent contractor.
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This is a fully remote opportunity with flexible scheduling.
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Projects may be extended, shortened, or concluded early depending on project requirements and performance.
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The engagement will not require access to confidential or proprietary information belonging to any employer, client, or institution.
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Payments are made weekly based on services rendered through available payment platforms.
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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.