Specialist Physician

Posted 14hrs ago

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Job Description

Board-certified US physicians evaluating clinical trials, medicines, and drug-development programmes for 24-MAG. Assessing prescribing impact, treatment adoption, and expert-review rubrics.

Responsibilities:

  • Review clinical trial results across relevant drug-development programmes
  • Interpret primary and secondary endpoints in the context of clinical practice
  • Assess the clinical significance of efficacy and safety findings
  • Evaluate whether trial outcomes are likely to influence treatment decisions
  • Apply disease-area expertise when interpreting complex clinical evidence
  • Determine whether new clinical evidence would meaningfully change prescribing behaviour
  • Compare emerging therapies with current standards of care
  • Evaluate treatment benefits, risks, patient selection, and practical prescribing considerations
  • Assess implications for treatment sequencing and therapeutic choices
  • Analyse commercial medicines and investigational drug programmes
  • Assess potential clinical differentiation and real-world uptake
  • Consider competitive treatment landscapes and evolving standards of care
  • Create structured evaluation rubrics for drug and clinical-development analysis
  • Critique existing rubrics for accuracy, completeness, and clinical relevance
  • Define criteria reflecting experienced physician judgment
  • Provide clear written reasoning supporting evaluation decisions
  • Participate in a focused paid pilot involving approximately 10–20 total hours over 1–2 weeks
  • Perform clinical-trial analysis, prescribing assessment, therapeutic-area evaluation, rubric development, and expert critique

Requirements:

  • MD or DO qualification is required
  • Board certification in the relevant medical specialty is required
  • Active clinical practice within a defined medical specialty is required
  • Deep expertise in a specific therapeutic or disease area
  • Strong familiarity with clinical trial endpoints and evidence interpretation
  • Experience translating clinical evidence into prescribing decisions
  • Familiarity with biotech or pharmaceutical development programmes
  • Strong understanding of real-world treatment adoption within the specialty
  • Excellent written communication and clinical reasoning skills
  • Current US-based clinical practice
  • Independent contractor status
  • Nice-to-have: experience serving as a clinical investigator
  • Nice-to-have: participation in pharmaceutical or biotechnology clinical trials
  • Nice-to-have: familiarity with drug-development strategy and pipeline assessment
  • Nice-to-have: experience reviewing clinical evidence for formulary, guideline, or treatment decisions
  • Nice-to-have: background advising pharmaceutical, biotechnology, or healthcare organisations
  • Nice-to-have: experience evaluating emerging therapies within a competitive treatment landscape
  • Nice-to-have: prior experience with structured expert review, rubric development, or AI evaluation

Benefits:

  • Competitive specialist compensation of $145–$225 per hour
  • Paid pilot with potential for recurring work
  • Weekly payments via Stripe or Wise
  • Strong contributors may be considered for recurring or expanded engagements
  • Work remotely
  • Projects may be extended, shortened, or adjusted depending on scope and performance