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I will write medical content and plain language summaries
Clinical Research Associate GCP Clinical Trial Documentation Specialist
I am a Clinical Research Associate (CRA) with 5 years of experience across global pharmaceutical and CRO studies - oncology, diabetes, dermatology, ophthalmology and more. I help international clients...
About this Gig
7 years as a Clinical Research Associate monitoring trials at CROs, GCP certified. I read your CSR, protocol or statistical output and write the version your audience understands.
WHAT I PRODUCE
- Plain-language summaries of trial results, ready for disclosure
- Patient information leaflets and consent explainers, English or Simplified Chinese
- HCP-facing content: slides, one-pagers, MSL discussion documents
- Literature and research summaries for non-specialist readers
- Website and brochure copy for clinics and startups
HOW I WORK
- Written from your documents. I do not invent numbers; every claim traces to a source you gave me
- Consistent with ICH-GCP and CONSORT conventions
- Tracked-changes draft plus a clean version
- Reading level set on request; patient-facing default is grade 8
I will not write health claims that outrun your data, and I do not fabricate citations.
Send me the source document and tell me who reads the finished piece.
Service type:
Summary
Language:
English
•
Chinese (simplified)
Delivery style preference
Please inform the freelancer of any preferences or concerns regarding the use of AI tools in the completion and/or delivery of your order.
Academic work to be done for you, is unethical since it violates most schools’ Honor Codes.
Asking sellers to prepare homework/academic works on your behalf is against Fiverr’s Community Standard and may lead to your account being disabled.
FAQ
Will my data stay confidential?
Nothing is published by me. I can sign an NDA before you send anything.
Can you work from Chinese source documents?
Yes. I read Chinese protocols, CRFs and statistical output and write in English.
