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









