
Clinical & Pharmaceutical Research Specialist
Posted Aug 21

Posted Aug 21
This is a fully remote position, open to applicants in New York.
• Evaluate work outputs related to clinical research and biomedical sciences.
• Assess the scientific accuracy, completeness, and consistency of the information presented.
• Identify unsupported assertions, factual inaccuracies, and gaps in clinical or scientific reasoning.
• Review whether conclusions appropriately reflect the existing evidence.
• Examine materials pertaining to pharmaceutical research, drug development, and associated scientific workflows.
• Assess the quality and credibility of analyses and recommendations.
• Interpret clinical findings, study results, and supporting evidence.
• Review spreadsheets, calculations, assumptions, tables, and supporting analyses.
• Evaluate scientific reports, spreadsheets, slide decks, technical presentations, charts, tables, and visuals.
• Assess assigned outputs against domain-specific quality criteria.
• Provide clear, structured written feedback that explains identified strengths and weaknesses.
• Apply evaluation standards consistently across various professional work products.
• 5+ years of relevant professional experience in clinical research, biomedical science, pharmaceutical research, drug development, or a closely related field.
• Strong practical understanding of clinical or biomedical research workflows.
• Ability to evaluate scientific evidence, data interpretation, and technical conclusions.
• Experience in reviewing research reports, clinical materials, scientific analyses, or pharmaceutical work products.
• Strong analytical judgment and attention to scientific detail.
• Highly proficient in Microsoft Office and Google Workspace.
• Advanced proficiency in PowerPoint / Google Slides.
• Strong spreadsheet and analytical skills.
• Native or professional fluency in English.
• Excellent written communication skills and the ability to provide precise, structured feedback.
• A Master's degree or higher from a recognized institution is advantageous.
• Work must be conducted without utilizing confidential or proprietary information from any employer, client, institution, or other third parties.
• H1-B and STEM OPT support is not available for this engagement.
• Part-time independent contractor engagement.
• Fully remote.
• Flexible scheduling based on project requirements.
• Projects may be extended, shortened, or concluded based on project needs and performance.
• H1-B and STEM OPT support is not available for this engagement.
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