Clinical Trial & Regulatory Medical Writer

Job not on LinkedIn

🔥 0 minutes ago

🌐 United States, Canada, +1 more countries – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote 🇫🇷 France – Remote

🗽 New York – Remote

🗽 New York – Remote

💵 $80 - $140 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

🏥📝 Medical Writer

👻 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

• Draft complete, publication-quality sections of Clinical Study Reports • Work across long-form clinical and regulatory documents requiring sustained consistency and technical accuracy • Translate clinical trial data into clear, structured scientific narratives • Ensure conclusions accurately reflect underlying study results • Maintain consistency across tables, analyses, terminology, and narrative sections • Review synthetic clinical trial datasets representing Phase I–III studies for accuracy, consistency, completeness, and plausibility • Identify inconsistencies, unsupported conclusions, or missing information • Validate whether written interpretations are appropriately supported by available data • Contribute to the creation of high-quality synthetic clinical trial data • Develop realistic study scenarios and data patterns grounded in clinical-development experience • Evaluate generated datasets for internal consistency and clinical credibility • Support quality-control processes for downstream research workflows • Design sophisticated medical-writing assignments based on realistic clinical workflows • Develop task instructions, expected deliverables, authoritative reference outputs, and objective evaluation criteria • Assess clinical narratives and regulatory documents for scientific accuracy, clarity, structure, traceability, and internal consistency • Identify fabricated, unsupported, or overstated claims and ensure appropriate professional judgement

🎯 Requirements

• 5+ years of professional medical-writing experience; 10–25 years preferred • Extensive hands-on experience with pre-market Phase I–III clinical trial data • Demonstrated experience authoring Clinical Study Reports (CSRs) and substantial sections of regulatory clinical documents • Comfortable owning full-document and long-horizon writing assignments • PhD or equivalent advanced academic/professional qualification • Strong understanding of clinical-development workflows and study-data interpretation • Ability to evaluate whether clinical conclusions are adequately supported by underlying evidence • Exceptional scientific writing, editing, and quality-control skills • Strong attention to detail across complex and lengthy documents • Able to work independently and maintain consistency across multiple concurrent workflows • Based in the United States, Canada, or France • Minimum availability of approximately 20–25 hours per week • Must not use confidential or proprietary information belonging to any employer, sponsor, client, institution, or other third party • H1-B and STEM OPT support is unavailable for this engagement

🏖️ Benefits

• Flexible scheduling based on project requirements • Fully remote work • Part-time independent contractor engagement • Availability of 30+ hours per week preferred • Projects may be extended, shortened, or concluded based on project needs and performance