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Fiverr Pro
Italiano
$
USD
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I will translate medical and clinical trial documents expertly
Cina
Parlo Cinese, Inglese
AI Automation Consultant
I help businesses automate workflows, analyze data, and build intelligent systems using AI. With 10+ years in clinical research operations, I bring domain expertise that pure tech freelancers lack.
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Informazioni su questo servizio
Medical translation isn't just about language it's about clinical accuracy. A wrong term in an ICF can delay your entire trial. With a Pharmacy degree and 10+ years of clinical trial experience, I deliver translations that regulatory reviewers trust.
What I translate:
Clinical Study Protocols & Amendments
Informed Consent Forms (ICF)
Investigator's Brochures (IB)
Case Report Forms (CRFs) & eCRF specifications
Regulatory submission documents (IND/NDA/BLA)
Medical device documentation
Clinical Study Reports (CSR)
SOPs, work instructions, training materials
My Unique Edge:
B.S. Pharmacy I understand the science, not just the words
10+ years clinical trial operations across Phase I-III
FDA/EMA/CFDA regulatory knowledge compliant terminology
Native Chinese + Advanced English (daily business communication)
AI-assisted QA process consistency check + medical terminology validation
Process: Translate Medical terminology QA Regulatory compliance check Client review Final delivery
Message me with your document I'll provide a free quote within 2 hours!
Lingua:
Inglese
•
Cinese (semplificato)
Tipo di documento:
Test farmaceutici/scientifici
Competenza settoriale:
Scienze naturali e mediche
Preferenza per lo stile di consegna
Informa il freelance di eventuali preferenze o preoccupazioni relative all'uso di strumenti di IA nel completamento e/o nella consegna dell'ordine.
FAQ
What types of medical documents can you translate?
I translate clinical study protocols, ICFs, investigator brochures, CRFs, regulatory submissions (IND/NDA/BLA), CSRs, SOPs, and medical device documentation.
Are you a certified medical translator?
I hold a B.S. in Pharmacy and have 10+ years of clinical trial experience across Phase I-III studies. My translations meet FDA/EMA/CFDA regulatory standards. I also use AI-assisted QA for terminology consistency.
What is your translation process?
My process: 1) Initial translation → 2) Medical terminology QA → 3) Regulatory compliance check → 4) Client review → 5) Final delivery. You receive a terminology glossary with Standard and Premium packages.
