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Specialised Part-Time Consulting OpportunityWe are sharing a specialised part-time consulting opportunity for board-certified, actively practising physicians with deep expertise in a defined therapeutic area and strong familiarity with clinical trials, prescribing decisions, and biotech or pharmaceutical development programmes.

This role supports an expert evaluation initiative focused on analysing commercial medicines and drug-development programmes. Selected clinicians will create and critique evaluation rubrics, interpret clinical trial endpoints, assess whether new evidence would meaningfully influence prescribing decisions, and evaluate the likely implications for real-world adoption within their therapeutic area.

Key ResponsibilitiesClinical Trial EvaluationReview clinical trial results across relevant drug-development programmesInterpret primary and secondary endpoints in the context of clinical practiceAssess the clinical significance of efficacy and safety findingsEvaluate whether trial outcomes are likely to influence treatment decisionsApply disease-area expertise when interpreting complex clinical evidencePrescribing & Treatment AssessmentDetermine whether new clinical evidence would meaningfully change prescribing behaviourAssess how emerging therapies compare with current standards of careEvaluate treatment benefits, risks, patient selection, and practical prescribing considerationsConsider how evidence may affect treatment sequencing or therapeutic choicesApply real-world clinical judgment rather than relying solely on headline trial resultsCommercial Drug & Pipeline ReviewAnalyse commercial medicines and investigational drug programmes within the relevant therapeutic areaAssess potential clinical differentiation and real-world uptakeEvaluate how trial results may influence physician adoptionConsider competitive treatment landscapes and evolving standards of careProvide expert perspective on the practical implications of development-stage evidenceRubric Development & Expert ReviewCreate structured evaluation rubrics for drug and clinical-development analysisCritique existing rubrics for accuracy, completeness, and clinical relevanceDefine criteria that reflect experienced physician judgmentIdentify missing considerations or misleading assumptions in analytical frameworksProvide clear written reasoning supporting evaluation decisionsIdeal ProfileStrong candidates may have: An MD or DOActive clinical practice within a defined medical specialtyBoard certification in the relevant specialtyDeep expertise in a specific therapeutic or disease areaStrong familiarity with clinical trial endpoints and evidence interpretationExperience translating clinical evidence into prescribing decisionsFamiliarity with biotech or pharmaceutical development programmesStrong understanding of real-world treatment adoption within their specialtyExcellent written communication and clinical reasoning skillsCurrent US-based clinical practiceEducational BackgroundMD or DO qualification is requiredBoard certification in the relevant medical specialty is requiredActive clinical practice is requiredAdditional research, academic, or clinical-trial experience may strengthen an applicationNice to HaveExperience serving as a clinical investigatorParticipation in pharmaceutical or biotechnology clinical trialsFamiliarity with drug-development strategy and pipeline assessmentExperience reviewing clinical evidence for formulary, guideline, or treatment decisionsBackground advising pharmaceutical, biotechnology, or healthcare organisationsExperience evaluating emerging therapies within a competitive treatment landscapePrior experience with structured expert review, rubric development, or AI evaluationWhy This OpportunityApply specialist clinical expertise to sophisticated drug-development evaluation workAnalyse trial endpoints through the lens of real prescribing decisionsAssess how new clinical evidence may influence treatment adoptionContribute expert judgment to evaluations of commercial and development-stage therapiesParticipate in a focused paid pilot with potential for recurring workWork remotely with competitive specialist compensationContract DetailsIndependent contractor roleFully remote within the United StatesPart-time pilot engagementApproximately 10–20 total hours over an initial 1–2 week periodCompetitive rates between $145–$225 per hour depending on expertise and project scopeStrong contributors may be considered for recurring or expanded engagementsWork may include clinical-trial analysis, prescribing assessment, therapeutic-area evaluation, rubric development, and expert critiqueWeekly payments via Stripe or WiseProjects may be extended, shortened, or adjusted depending on scope and performanceWork will not involve access to confidential or proprietary information from any employer, client, or institutionAbout the PlatformThis opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.

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