Clinical & Pharmaceutical Research Specialist

Job not on LinkedIn

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🗽 New York – Remote

🗽 New York – Remote

💵 $70 - $110 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

🔬 Research Analyst

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Evaluate work products involving clinical research and biomedical science • Assess scientific accuracy, completeness, and consistency of presented information • Identify unsupported claims, factual errors, and gaps in clinical or scientific reasoning • Review whether conclusions appropriately reflect available evidence • Review materials involving pharmaceutical research, drug development, and related 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 explaining identified strengths and weaknesses • Apply evaluation standards consistently across different professional work products

🎯 Requirements

• 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 reviewing research reports, clinical materials, scientific analyses, or pharmaceutical work products • Strong analytical judgement and attention to scientific detail • Highly proficient with Microsoft Office and Google Workspace • Advanced proficiency with PowerPoint / Google Slides • Strong spreadsheet and analytical skills • Native or professional fluency in English • Excellent written communication and ability to provide precise, structured feedback • Master's degree or higher from a recognised institution is advantageous • Work must be completed without using confidential or proprietary information belonging to any employer, client, institution, or other third party • H1-B and STEM OPT support is unavailable for this engagement

🏖️ Benefits

• 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 unavailable for this engagement