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.