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Responsibilities
• Translate, post‑edit and review clinical trial documentation to ensure they adhere to medical and ethical standards.
• Enhance the readability, accuracy, and coherence of scientific and medical materials without altering the original meaning.
• Collaborate with translation teams to provide constructive feedback and suggest necessary corrections.
• Stay updated with the latest terminology and advancements in the medical field.
Requirements
• Proven experience in clinical translation/post‑editing.
• Native fluency in the target language.
• Fluency in the source language(s).
• Strong attention to detail and commitment to accuracy.
• Excellent written communication skills.
• A deep understanding of clinical terminology and concepts.
• Ability to work independently and meet deadlines.
• Certification in medical post‑editing, translation, or a related discipline (preferred).
• Experience with memoQ (preferred).
• A medical/pharma degree would be a plus (preferred).
Hard Skills
• clinical translation
• post‑editing
• medical terminology
• scientific writing
Soft Skills
• attention to detail
• commitment to accuracy
• written communication
• independence
• time management
Certifications & Qualifications
• medical post‑editing certification
• translation certification
Industry Keywords
• clinical trial documentation
• medical standards
• ethical standards
Tools & Technologies
• memoQ
