This role is for one of our clientsCompensation: $150 - $230 per hourWe 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.RequirementsKey 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 OpportunityWe consider all qualified applicants without regard to legally protected characteristics and provide reasonable accommodations upon request.
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.
At Weekday (backed by YC; also Product Hunt #1 product of the day), we are building the next frontier in hiring. We have built the largest database of white collar talent in India and have built outreach tools on top of it to generate highest response rates.
At Weekday (backed by YC; also Product Hunt #1 product of the day), we are building the next frontier in hiring. We have built the largest database of white collar talent in India and have built outreach tools on top of it to generate highest response rates.
