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Linguamatics

Freelance Medical/Legal Post-Editors, English-Latvian

Linguamatics

. Translate, post-edit and review clinical trial documentation to ensure adherence to target-language medical and ethical standards .

Posted 11/5/2026contractRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in translating and post-editing clinical trial documentation while ensuring compliance with medical and ethical standards. Possesses native fluency in Latvian and fluency in English, with a strong understanding of clinical terminology and concepts.

Highest-signal resume keywords
Native Fluency In LatvianFluency In EnglishCertification In Medical Post-EditingExperience With MemoQDeep Understanding Of Clinical Terminology

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Translation Of Clinical Trial DocumentationPost-Editing Of Scientific MaterialsReviewing Medical DocumentsEnhancing Readability And AccuracyAdherence To Regulatory Requirements
Soft Skills
Strong Attention To DetailExcellent Written Communication SkillsAbility To Work IndependentlyCommitment To AccuracyConstructive Feedback
Tools & Technologies
MemoQ
Certifications & Qualifications
Certification In Medical Post-EditingCertification In Translation
Industry Keywords
Clinical ResearchMedical TerminologyEthical StandardsRegulatory ComplianceIQVIA Core Values

About the role

Key responsibilities & impact
  • Translate, post-edit and review clinical trial documentation to ensure adherence to target-language 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
  • Ensure all documents comply with applicable regulatory requirements and guidelines

Requirements

What you’ll need
  • Proven experience translating legal documents related to clinical research
  • Native fluency in Latvian
  • Fluency in English
  • Strong attention to detail and commitment to accuracy
  • Excellent written communication skills
  • 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)
  • Adherence to IQVIA core values: Client-focus, Collaboration, Communication, Ownership and Innovation
  • A Medical/Pharma degree would be a plus

Benefits

Comp & perks
  • Competitive payment terms
  • Flexible scheduling
  • Training for continuous development
  • Opportunity to work on a variety of interesting projects
  • Supportive community of language and medical professionals