I will write format clinical study report regulatory medical documents for cros pharma

United Kingdom

I speak English, French, German, Spanish

Medical Writer Clinical, Regulatory And Health Book Ghostwriting And Formatting

Hi, I'm Marcus, a medical writer specializing in both clinical/regulatory documentation and health book ghostwriting. I write and format Clinical Study Reports, regulatory submissions, and CME content...
About this Gig

Need a document that's both scientifically accurate and submission-ready?


I combine clinical/medical writing expertise with precise formatting to deliver documents that meet regulatory, journal, or internal compliance standards no back-and-forth needed to fix structure, citations, or layout.


I can help with:

  • Clinical study reports (CSRs)
  • Regulatory submission documents
  • Manuscript preparation for journal submission (journal-specific formatting + citation styles: AMA, Vancouver, APA)
  • Patient education materials & informed consent forms
  • CME (continuing medical education) content
  • Protocol writing and summaries


Why work with me:

  • Content that respects clinical accuracy and liability standards
  • Formatting done right the first time (headers, tables, references, version control)
  • Fast turnaround with clear revision rounds
  • Confidentiality guaranteed (NDA on request)


Let's get your document submission-ready.

Send me your project details or raw materials, and I'll turn them into a clean, accurate, properly formatted document built to the standard your reviewers or regulators expect.


Order now or message me now and I'll help you pick the right package.

Document type:

Reports

Regulatory Documents

Industry:

Medical & biotech

Language:

English

Spanish

Delivery style preference

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