French to English Life Sciences, Pharmacovigilance Linguist

Job not on LinkedIn

🕒 July 31

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟢 Junior

🟡 Mid-level

👻 Ghost score 18%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Welo Global

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🤖 Artificial Intelligence

🤝 B2B

☁️ SaaS

Artificial Intelligence • B2B • SaaS

Welo Global is a multilingual content, data, and AI solutions company that provides enterprise-focused localization, regulated translation, and AI training data through a family of brands (including Welocalize, Park IP, Welo Life Sciences, Welo Data, and Adapt). It combines domain expertise, proprietary AI tools (e. g. , the Opal suite), governed global workforces, and compliance certifications to support use cases across global marketing, intellectual property and legal translations, life sciences regulatory and clinical documentation, and AI model development. The company emphasizes scalable, AI-enabled platforms and workflows to deliver high-quality multilingual content and structured datasets in 300+ languages for corporate clients.

📋 Description

• We are looking for experienced French (France) to English (GB and US) linguists to support a high-volume, fast-turnaround pharmacovigilance program for a leading global pharmaceutical company. • Work involves translating and reviewing safety and regulatory content, including adverse event reports and related clinical documentation, with strict turnaround times and deadlines. • This is an ongoing freelance engagement with daily volumes. • Translate pharmacovigilance and/or clinical-regulatory content from French into English. • Perform Machine Translation Post-Editing (MTPE) on machine-translated safety content. • Perform Copy Edit review of translated/post-edited content for accuracy, tone, and consistency. • Meet strict, non-extendable turnaround times on time-sensitive safety content. • Occasionally support Transcription tasks, retyping scanned or handwritten PDFs into Word for downstream translation (requires a personal Gmail account for client platform access). • Work within the client's CAT tool environment (XTM) following project-specific setup instructions.

🎯 Requirements

• Degree in translation, linguistics or languages studies or an equivalent degree that includes significant • translation training. • Minimum 2 years of professional experience translating Life Sciences documents. • Experience translating pharmacovigilance content preferred: SAE/AE (serious and non-serious adverse events), PSURs, SUSARs, ICSRs, DSURs, Risk Management Plans (RMP). • Alternatively, experience translating regulatory or clinical documents: medical reports, protocols, synopses, ICF, discharge reports, study reports, SmPC, PIL, or medical literature. • Great daily availability: this program requires consistent daily capacity and is not suited to part-time schedules. • Strong English proficiency; native level of English preferred but not mandatory. • Experience with XTM or similar CAT tools. • Reliable, deadline-driven, and flexible, able to commit to fast turnaround times with no extensions. • Nice to Have: Healthcare professional (HCP) background: nurse or physician preferred, especially with emergency room experience. • Availability to cover US business hours. • Willingness to commit to daily and/or weekend availability.