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English to Hungarian Linguist for Life Sciences

AI Summary
Welo Life Sciences is seeking an experienced English-to-Hungarian freelance linguist for regulated life-sciences content. The role covers translation, machine-translation post-editing, and copy editing of clinical-trial, pharmacovigilance, and regulatory documents. The linguist will work in client CAT-tool environments, including XTM or Phrase, and use Microsoft Word Track Changes while meeting strict turnaround times. Candidates need demonstrable medical and life-sciences translation experience, strong Hungarian-language expertise, and a willingness to complete an onboarding assessment.
Remote from
Hungary
Salary
Undisclosed
Employment
Contract
Experience
Open level
Published
Apply before
12 Dec 2026
Listing views
30
Application actions
0
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Opportunity details

About this role.

About Welo Life Sciences

Welo Life Sciences, a Welo Global brand, is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations operating in regulated global markets. We deliver regulator-ready translation, linguistic validation, and localization solutions that support clinical trials, pharmacovigilance, regulatory affairs, labeling, and global commercialization. Our approach combines subject matter expertise with ISO-certified quality processes and technology-enabled workflows designed to integrate seamlessly into life sciences operations. With extensive experience supporting global product development and post-market requirements, Welo Life Sciences helps organizations accelerate timelines, protect data integrity, and maintain compliance across languages and regions. All solutions are delivered within a secure, audit-ready framework supported by seven ISO certifications. welolifesciences.com

About the Role

We are looking for experienced English into Hungarian linguists specializing in Clinical-trial, Pharmacovigilance and Regulatory document translation.

Key Responsibilities

  • Translate clinical research, regulatory and pharmacovigilance documents from English to Hungarian.
  • Perform Machine Translation Post-Editing (MTPE) on machine-translated safety content.
  • Perform Copy Edit (translation review) of translated/post-edited content for accuracy, tone, and consistency.
  • Meet strict, non-extendable turnaround times on time-sensitive content.
  • Work within the client’s CAT tool environment (XTM/Phrase), also Track Changes in Microsoft Word following project-specific setup instructions.

Field of Expertise

  • Clinical Research Documents (protocols and synopses, IB, ICF, Patient Sheets, Patient Diaries)
  • Regulatory Documents (SmPC, PIL, Labels, CTD Modules)
  • Pharmacovigilance Documents (PSUR, DSUR, RMP, SAE and AE)

Must-Have Criteria

  • Applicant must meet at least one of the following criteria:

Education

  • A degree in Translation, Linguistics, or Language Studies (or an equivalent degree) or
  • Recognized graduate qualification in any other field, plus a minimum of two years of full-time professional experience in translation or
  • A minimum of five years of full-time professional experience in translation

Relevant translation experience

  • At least two years of practical translation experience, specifically with life sciences (clinical trials and pharmacovigilance) and medical documents

Technical Skills

  • Familiarity with CAT tools (XTM/Phrase), License will be provided.
  • Familiarity with Track Changes in Microsoft Word

Nice-to-Have

  • Degree in Medicine, Biology, Biochemistry, Clinical Research, Translation, Linguistics, Philology or similar
  • In-house industry experience at a CRO or pharmaceutical company.

Before Applying

Please note there will be an assessment as part of our onboarding and quality procedure, please only apply if you’re willing to complete our assessment.

Please ensure your latest English CV accurately reflects your Life Sciences and Medical translation experience, including years of experience specifically in Life Sciences, the document types you’ve translated, CAT tool you’ve used, and relevant details also your contact information (email AND phone number).

Beware of recruitment scams. Welo Global and all of its brands never recruit through direct messages on social media or WhatsApp, and never asks candidates to pay money for a job. Official emails come only from @welocalize.com, @welodata.ai, or @hire.lever.co, and all applications go through jobs.lever.co/weloglobal. Be wary of unexpected offers, generic email addresses (such as Gmail or Yahoo), and requests for fees or sensitive information. Report suspicious messages and learn more: Recognizing Scams and Confirming Legitimate Welocalize Communications – Welo Global

We look forward to receiving your application!

Job Reference: #LI-JC1

Compensation

Additional Information

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This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content.

Role DNA

A quick view of the complexity, pace, ownership and collaboration implied by the job description.

Job Complexity

4/5
EasyHard

Pace & Pressure

4/5
RelaxedFast-paced

Autonomy Level

4/5
GuidedFull ownership

Communication Load

3/5
IndependentCollaborative
AI insightThis is a specialized regulated-content translation role where terminology accuracy can affect clinical, safety, and regulatory outcomes. It requires proven subject-matter knowledge as well as disciplined quality control under firm deadlines.

Salary analysis

Estimated compensation compared with the broader US market for similar roles.

Estimated job median (per hour)Highly competitive
$35
US market range (per hour)$25–$45
AI insightThe hourly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer compensation was disclosed. The hourly cadence is inferred from the freelance remote linguist arrangement; the estimated USD 25–45 hourly market range reflects specialized English-to-Hungarian life-sciences translation, MTPE, and review work.

Core skills

Skills and capabilities most closely associated with this opportunity.

Sample interview questions
How do you maintain accuracy when translating clinical-trial and pharmacovigilance documents?

I first identify the document type, target audience, and applicable terminology sources. I use approved glossaries and reference materials, verify clinical and safety terminology, and perform a structured final review for meaning, consistency, numbers, units, and formatting.

Describe your experience with machine translation post-editing for regulated content.

I assess whether the machine output preserves the source meaning, clinical terminology, and required register before editing it. I correct mistranslations, omissions, terminology inconsistencies, and Hungarian grammar while ensuring the final text meets the same quality standard as human translation.

How would you handle a tight, non-extendable turnaround time for a safety document?

I would confirm scope and priorities immediately, prepare terminology and reference files, and plan focused translation and review stages. I would communicate early if a source issue could affect quality or timing, while maintaining a final quality-control pass before delivery.

What is your approach to reviewing another linguist's Hungarian translation?

I compare the target text against the source for completeness, accuracy, terminology, style, and regulatory appropriateness. I use Track Changes and concise comments to make edits transparent, prioritizing objective corrections and project-specific conventions.

Which information would you include in a CV for this role?

I would clearly state my English-to-Hungarian life-sciences experience, years of professional translation work, relevant clinical and pharmacovigilance document types, education, CAT tools, quality-review experience, and current contact details.

This analysis is generated from the job description. Salary estimates, role characteristics and sample answers are guidance, not employer-provided facts.
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