About The Position

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.

Requirements

  • 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.

Nice To Haves

  • 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.

Responsibilities

  • 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.

Benefits

  • Competitive hourly compensation
  • Remote structure with flexible scheduling
  • Weekly payments via Stripe or Wise
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