Remote

We are sharing a specialised part-time consulting opportunity for clinical, biomedical, and pharmaceutical professionals experienced in reviewing clinical research materials, biomedical documents, pharma summaries, study reports, medical content, evidence reviews, spreadsheets, slide decks, and presentation-ready life sciences artifacts for accuracy, rigor, clarity, and domain quality.

This role supports current and upcoming remote consulting opportunities focused on clinical and biomedical artifact review, pharma materials evaluation, rubric-based assessment, document and spreadsheet review, slide deck quality review, structured feedback, and high-quality project execution. Selected professionals will evaluate AI-generated work products and apply subject-matter expertise to identify factual, scientific, clinical, analytical, aesthetic, and presentation issues.

Key Responsibilities

Professionals in this role may contribute to:

Clinical & Biomedical Artifact Review

• Evaluate AI-generated documents, spreadsheets, and slide decks involving clinical research, biomedical science, pharmaceutical materials, therapeutic areas, study summaries, evidence reviews, and medical content
• Review clinical and biomedical materials for accuracy, completeness, rigor, clarity, and practical relevance
• Assess whether scientific claims are supported by appropriate evidence, methodology, assumptions, and domain context
• Identify inaccurate claims, weak study interpretation, unclear clinical logic, incomplete evidence review, or poor linkage between findings and conclusions

Pharma & Scientific Quality Evaluation

• Review materials involving clinical trial summaries, safety and efficacy discussions, therapeutic area overviews, medical affairs materials, literature summaries, product-related scientific materials, and healthcare-facing presentations
• Assess whether pharma and life sciences materials are clear, well-structured, scientifically sound, and appropriate for professional audiences
• Evaluate spreadsheets, evidence tables, study comparison materials, scientific summaries, and executive-facing recommendations for rigor and usability
• Provide clear written feedback that improves clinical, biomedical, and pharma artifact quality

Spreadsheet, Document & Presentation Quality Review

• Review spreadsheets for structure, logic, calculations, formatting, usability, and consistency
• Assess slide decks for organization, visual clarity, executive readability, and presentation quality
• Identify factual, aesthetic, formatting, and presentation errors across Microsoft Office and Google Workspace files
• Apply consistent review standards across documents, spreadsheets, and slide decks

Ideal Profile

Strong candidates may have:

• 5+ years of relevant professional experience in clinical research, biomedical science, pharmaceutical work, medical affairs, life sciences research, clinical development, medical writing, healthcare consulting, regulatory science, or related fields
• Native or professional fluency in English
• High proficiency in Microsoft Office and Google Workspace
• Strong experience with Google Slides, PowerPoint, Excel, Google Sheets, Word, and Google Docs
• Ability to evaluate documents, spreadsheets, and slide decks with strong attention to detail
• Excellent written communication skills and ability to provide structured feedback
• Ability to work independently in a remote, project-based environment

Educational Background

• Academic backgrounds in medicine, pharmacy, biomedical science, clinical research, public health, pharmacology, biology, biochemistry, molecular biology, pharmaceutical sciences, or related fields may be relevant
• Advanced degree from a reputable institution may be valuable
• Professional training in clinical research, medical writing, evidence review, pharmaceutical science, regulatory science, or therapeutic area analysis may also be relevant depending on project scope

Nice to Have

• MD, PharmD, PhD, MPH, MSc, or comparable clinical, biomedical, or pharmaceutical credential
• Experience creating or reviewing clinical study summaries, literature reviews, evidence tables, therapeutic area materials, medical affairs decks, safety/efficacy summaries, regulatory science materials, or healthcare-facing presentations
• Familiarity with clinical trial design, GCP, study endpoints, evidence hierarchy, therapeutic area research, pharmacology, medical claims review, and scientific communication standards
• Experience reviewing presentation decks for clarity, polish, and life sciences communication quality
• Strong ability to evaluate both scientific substance and visual/presentation quality

Why This Opportunity

• Apply clinical, biomedical, and pharma expertise to structured remote evaluation work
• Review high-quality documents, spreadsheets, and slide decks across clinical research, biomedical science, pharmaceutical materials, and evidence review topics
• Contribute to accurate, rigorous, and professionally presented life sciences materials
• Use your scientific and clinical judgment to improve artifact quality
• Remote structure with competitive hourly compensation

Contract Details

• Independent contractor role
• Fully remote with flexible scheduling
• Eligible professionals may be based in approved project locations depending on project needs
• Project commitment may vary depending on availability and scope
• Competitive rates between $70–$110 per hour depending on expertise and project scope
• Weekly payments via Stripe or Wise
• Projects may be extended, shortened, or adjusted depending on scope and performance
• Work will not involve access to confidential or proprietary information from any employer, client, or institution

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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