Specialist Physician

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🗽 New York – Remote

🗽 New York – Remote

💵 $145 - $225 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

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24-MAG

WebsiteLinkedInAll Job Openings

2 - 10 employees

🤝 B2B

💼 Consulting

B2B • Consulting

24-MAG is a commercial strategy and execution firm that helps B2B organizations design and implement systems, workflows, and operating rhythms for sales, client management, and cross-functional projects. They focus on transforming scattered processes into aligned, measurable, and scalable commercial functions—covering pipeline structure, account management frameworks, and operational discipline for teams seeking efficient, intentional growth.

📋 Description

• 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