出海雷达

English to Spanish (ESUS/US based) Linguist for Life Sciences

其他全球可投
公司Welo Global
薪资未公开
工作地点Remote, Worldwide
地域资格全球可投
时区要求无特别要求
用工类型Freelance-Remote
发布时间未知
数据来源Lever
前往企业招聘页投递 →
全球可投:该职位未限制候选人所在地区。仍需注意薪资可能按地区折算,以及实际签约方式(正式雇佣 / 独立合同)。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

关于韦洛生命科学,威洛全球品牌是专门服务于在监管的全球市场上运营的制药,CRO 和医疗设备组织的语言和技术合作伙伴。我们提供准备好调控器的翻译,语文验证和本地化解决方案,支持临床试验,药物警,监管事务,标签和全球商业化。我们的方法结合了相关专业知识与 ISO 认证质量流程以及旨在无整合到生物科学运作中的技术启用工作流程。凭借支持全球产品开发和市场后需求的丰富经验,Welo Life Sciences 帮助组织加速时间表,保护数据完整性并保持跨语言和地区的合规性。所有解决方案都在7项 ISO 认证所支持的安全,审计准备框架内提供.welolifesciences.com 关于角色 我们正在寻找专业于临床试验,药物警和监管文档翻译的有经验的英语到西班牙语 (ESUS/美国)语言学家。关键责任 · 从英文转换临床研究,监管和药物警?? 文档。· 执行机器翻译后编辑 (MTPE) 在机器翻写安全内容。· 对翻译/经过编辑的内容进行复制编辑 (翻译审查)以确保准确性,语调和一致性。·满足对时间敏感内容的严格,不可延伸的转换时间。· 在客户的 CAT 工具环境中工作 (XTM/Phrase),同时跟踪 Microsoft Word 中的变化,遵循项目特定设置说明。专业知识领域 ·临床研究文件 (协议和综合,IB,ICF,患者单片,病人的日志)·监控文件 (SmPC,PIL,标签,CTDules)·监督标准 (PSUR,药品,RMP,SAE 和 AE-Have). · 申请人必须满足以下标准之一:教育·翻译,语言学或语言研究学位 (或相等程度)或 · 在任何其他领域的认可毕业资格,加上至少两年全职翻译专业经验;• 具有相关翻译经验;• 拥有至少两年的实践翻译经历,特别是生命科学 (临床试验和药物警);

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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 Spanish (ESUS/US based) linguists specializing in Clinical-trial, Pharmacovigilance and Regulatory document translation.

Key Responsibilities

  • Translate clinical research, regulatory and pharmacovigilance documents from English to Spanish LatAm.
  • 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

Native Language

  • Candidates must be native Spanish speakers who were born and raised in the U.S., or have been residing in the U.S. for at least 10 years and be able to demonstrate familiarity with the differences between the Spanish used in their country of origin and in the U.S.

Location

  • A candidate must be based in the U.S.

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).

We look forward to receiving your application!

Job Reference: #LI-JC1

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