Spanish (Spain) to English Pharmacovigilance Linguist

<p><strong>About Welo Life Sciences</strong> </p> <p>Welo Life Sciences, a <a href="https://jobicy.com/company/welo-global" target="_blank" rel="noopener">Welo Global</a> 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. <a href="https://www.welolifesciences.com/" rel="nofollow ugc noopener" target="_blank"><em>welolifesciences.com</em></a></p> <h3>About the Role</h3> <p>We are looking for experienced <strong>Spanish (Spain) to English (GB or US) </strong>linguists to support a high-volume, fast-turnaround <strong>pharmacovigilance </strong>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. </p> <p>This is an ongoing freelance engagement with daily volumes.</p> <h3>Key Responsibilities</h3> <ul> <li>Translate Pharmacovigilance and/or Clinical-regulatory content from Spanish into English.</li> <li>Perform Machine Translation Post-Editing (MTPE) on machine-translated safety content.</li> <li>Perform Copy Edit review of translated/post-edited content for accuracy, tone, and consistency.</li> <li>Meet strict, non-extendable turnaround times on time-sensitive safety content.</li> </ul> <h3>Requirements</h3> <ul> <li>Degree in translation, linguistics or languages studies or an equivalent degree that includes significant <br>translation training.</li> <li><strong>Minimum 2 years of professional experience translating medical documentation, specificially with experience and knowledge in Pharmacovigilance and/or Clinical-Regulatory content.</strong></li> <li>Experience translating pharmacovigilance content preferred: SAE/AE (serious and non-serious adverse events), PSURs, SUSARs, ICSRs, DSURs, Risk Management Plans (RMP).</li> <li>Alternatively, experience translating regulatory or clinical documents: medical reports, protocols, synopses, ICF, discharge reports, study reports, SmPC, PIL, or medical literature.</li> <li>Great daily availability: this program requires consistent daily capacity and is not suited to part-time schedules.</li> <li>Strong Spanish profic