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Welo Life Sciences, a Welo Global brand, seeks experienced English-to-Spanish translators based in the United States for clinical-trial, pharmacovigilance, and regulatory document translation. You will translate and post-edit regulatory and pharmacovigilance documents, meeting tight deadlines and working within XTM/Phrase and Word Track Changes workflows.
Applicants should have strong translation experience in life sciences and a relevant degree; familiarity with CAT tools and MS Word is
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.
We are looking for experienced
English into Spanish (US based)
linguists specializing in
Clinical-trial,
Pharmacovigilance and Regulatory
document translation.
Translate clinical research, regulatory and pharmacovigilance documents from English to Spanish LatAm.
Applicant must meet at least one of the following criteria:
Job Reference: #LI-JC1