Specialist Physician

This is a fully remote position, open to applicants in New York.

📋 Description

• Review clinical trial outcomes across pertinent drug-development initiatives.

• Interpret both primary and secondary endpoints within the framework of clinical practice.

• Evaluate the clinical relevance of efficacy and safety results.

• Determine if trial results are likely to affect treatment choices.

• Utilize disease-area expertise when analyzing intricate clinical data.

• Assess whether new clinical insights will significantly alter prescribing habits.

• Compare new therapies with existing standards of care.

• Evaluate treatment advantages, risks, patient selection, and practical prescribing factors.

• Analyze implications for treatment sequencing and therapeutic options.

• Review commercial medications and investigational drug programs.

• Examine potential clinical differentiation and real-world adoption.

• Take into account competitive treatment environments and evolving standards of care.

• Develop structured evaluation frameworks for drug and clinical development assessment.

• Critique existing frameworks for precision, thoroughness, and clinical relevance.

• Establish criteria that reflect the judgment of experienced physicians.

• Provide clear written justifications for evaluation conclusions.

• Engage in a focused paid pilot requiring approximately 10–20 total hours over 1–2 weeks.

• Conduct clinical trial analysis, prescribing evaluations, therapeutic area assessments, rubric development, and expert critiques.

⛳️ Requirements

• An MD or DO qualification is mandatory.

• Board certification in the relevant medical specialty is necessary.

• Active clinical practice in a defined medical specialty is required.

• Extensive expertise in a specific therapeutic or disease area.

• Strong knowledge of clinical trial endpoints and evidence interpretation.

• Experience in translating clinical evidence into prescribing choices.

• Familiarity with biotech or pharmaceutical development programs.

• Comprehensive understanding of real-world treatment adoption in the specialty.

• Exceptional written communication and clinical reasoning capabilities.

• Current clinical practice based in the US.

• Must hold independent contractor status.

• Nice-to-have: experience as a clinical investigator.

• Nice-to-have: involvement in pharmaceutical or biotechnology clinical trials.

• Nice-to-have: knowledge of drug-development strategy and pipeline evaluation.

• Nice-to-have: experience reviewing clinical evidence for formulary, guideline, or treatment decisions.

• Nice-to-have: background in advising pharmaceutical, biotechnology, or healthcare organizations.

• Nice-to-have: experience assessing emerging therapies within a competitive treatment framework.

• Nice-to-have: prior experience with structured expert review, rubric development, or AI evaluation.

🏝️ Benefits

• Competitive specialist compensation ranging from $145 to $225 per hour.

• Paid pilot with the potential for ongoing work opportunities.

• Weekly payments processed through Stripe or Wise.

• High-performing contributors may be considered for ongoing or expanded roles.

• Opportunity to work remotely.

• Project durations may be extended, shortened, or modified based on scope and performance.