Disease-Area Clinician — Trial Endpoints & Prescribing

Position Type: Part-Time Contract
Location: Remote — United States
Compensation: $150–$230/hour
Engagement: Approximately 10–20 hours over a 1–2 week pilot

About the Role

We are seeking an experienced disease-area clinician to support expert evaluation work focused on commercial drugs and drug-development programs.

You will apply your clinical expertise to assess clinical trial results, develop and critique evaluation rubrics, and determine how evidence from clinical trials could influence real-world prescribing and treatment decisions within your therapeutic area.

The engagement begins with a short paid pilot, with potential for recurring work as the project expands.

Key Responsibilities

• Create and critique rubrics for evaluating commercial drugs and drug-development programs.

• Interpret clinical trial endpoints and assess the significance of reported results.

• Evaluate whether trial outcomes are likely to influence prescribing decisions.

• Assess the potential implications of clinical evidence for real-world treatment uptake within your therapeutic area.

• Apply your disease-area expertise consistently across assigned drugs and development programs.

Requirements

• US-based practicing physician (MD/DO).

• Board-certified and actively practicing in your specialty.

• Deep clinical expertise in a specific therapeutic or disease area.

• Familiarity with biotech and pharmaceutical drug-development programs.

• Strong ability to interpret clinical evidence and connect trial outcomes to real-world clinical practice.

• US market experience is required.

Engagement Details

• Format: Fully remote

• Initial engagement: Approximately 10–20 hours

• Pilot duration: 1–2 weeks

• Potential: Recurring opportunities for strong contributors

• Schedule: Flexible, subject to project requirements

• Contract: Independent contractor

Why Participate?

• Apply your clinical expertise to emerging approaches to AI evaluation.

• Help improve expert-level assessment of drugs and drug-development programs.

• Contribute practical clinical perspectives on how evidence translates into prescribing and treatment decisions.

• Potential for continued engagement as the work scales.

Contract & Payment Terms

• Projects may be extended, shortened, or concluded early based on project needs and performance.

• Work will not involve access to confidential or proprietary information from any employer, client, or institution.

• Payments are made weekly through Stripe or Wise based on services rendered.

• H1-B and STEM OPT candidates cannot be supported at this time.

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