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.
