We are sharing a specialised part-time consulting opportunity for experienced clinical, biomedical, and pharmaceutical professionals with strong expertise in scientific analysis, clinical research, evidence interpretation, and professional work-product review.
This role focuses on reviewing professional documents, spreadsheets, and presentation materials involving clinical, biomedical, and pharmaceutical topics. Selected experts will assess outputs for scientific accuracy, analytical rigour, evidentiary support, presentation quality, and overall professional credibility.
Key Responsibilities
Clinical & Biomedical Review
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Evaluate work products involving clinical research and biomedical science
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Assess scientific accuracy, completeness, and consistency of presented information
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Identify unsupported claims, factual errors, and gaps in clinical or scientific reasoning
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Review whether conclusions appropriately reflect the available evidence
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Apply professional judgement to realistic clinical and biomedical scenarios
Pharmaceutical Research & Analysis
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Review materials involving pharmaceutical research, drug development, and related scientific workflows
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Assess the quality and credibility of analyses and recommendations
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Identify inaccurate assumptions or inconsistencies in pharmaceutical content
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Evaluate whether scientific conclusions are appropriately supported
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Review complex technical information for professional accuracy and usability
Clinical Evidence Interpretation
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Evaluate interpretation of clinical findings, study results, and supporting evidence
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Assess whether conclusions are proportionate to the underlying data
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Identify overstatement, unsupported causal claims, or incomplete interpretation
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Review consistency between quantitative findings and written conclusions
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Evaluate how effectively uncertainty and limitations are communicated
Scientific Data & Spreadsheet Review
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Assess spreadsheets containing clinical, biomedical, or pharmaceutical data
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Review calculations, assumptions, tables, and supporting analyses for consistency
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Identify discrepancies between underlying data and reported findings
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Evaluate whether quantitative information is represented clearly and accurately
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Ensure conclusions remain traceable to supporting evidence
Documents & Presentation Review
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Evaluate scientific reports, spreadsheets, and slide decks for accuracy and completeness
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Review technical and stakeholder presentations for clarity and logical flow
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Identify factual, analytical, aesthetic, and formatting issues
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Assess whether charts, tables, and visuals accurately represent underlying information
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Ensure scientific findings and recommendations are communicated clearly
Structured Evaluation & Feedback
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Assess assigned outputs against domain-specific quality criteria
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Identify scientific, factual, analytical, and presentation errors
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Distinguish substantive domain issues from minor editorial concerns
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Provide clear, structured written feedback explaining identified strengths and weaknesses
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Apply evaluation standards consistently across different professional work products
Ideal Profile
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5+ years of relevant professional experience in clinical research, biomedical science, pharmaceutical research, drug development, or a closely related field
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Strong practical understanding of clinical or biomedical research workflows
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Ability to evaluate scientific evidence, data interpretation, and technical conclusions
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Experience reviewing research reports, clinical materials, scientific analyses, or pharmaceutical work products
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Strong analytical judgement and attention to scientific detail
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Highly proficient with Microsoft Office and Google Workspace
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Advanced proficiency with PowerPoint / Google Slides
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Strong spreadsheet and analytical skills
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Native or professional fluency in English
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Excellent written communication and ability to provide precise, structured feedback
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Master's degree or higher from a recognised institution is advantageous
Engagement Details
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Part-time independent contractor engagement
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Fully remote
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Flexible scheduling based on project requirements
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Compensation: $70–$110/hour
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Work includes evaluation of clinical, biomedical, and pharmaceutical documents, spreadsheets, and presentation materials
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Projects may be extended, shortened, or concluded based on project needs and performance
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Work must be completed without using confidential or proprietary information belonging to any employer, client, institution, or other third party
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H1-B and STEM OPT support is unavailable for this engagement
About the Platform
This 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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