Responsibilities
- Post-edit and review clinical trial documentation to ensure they adhere to the target language's 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 to ensure translations are current and accurate
- Ensure all documents comply with applicable regulatory requirements and guidelines
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, or a related discipline (preferred)
- A Medical/Pharma degree would be a plus (preferred)
Hard Skills
- clinical translation
- post-editing
- medical terminology
- scientific writing
- accuracy
- readability enhancement
- coherence improvement
Soft Skills
- attention to detail
- written communication
- independence
- deadline management
- collaboration
- constructive feedback
Certifications & Qualifications
- medical post-editing certification
Industry Keywords
- clinical trial documentation
- regulatory requirements
- ethical standards
- medical field advancements
- target language
- source language
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