出海雷达

临床试验助理 II

Clinical Trials Assistant II

其他限定地区(需当地身份)
公司Lifelancer
薪资未公开
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间14 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

职位名称:临床试验助理 II
工作地点:英国伯克郡雷丁
工作地点类型:远程
雇佣类型:全职
职级:
加入IQVIA,助力加速创新,创造更健康的世界!

作为临床试验助理(CTA I 或 CTA II),您将通过保持准确的文件记录、协调研究活动,帮助确保项目符合规范并按计划进行。与临床研究专员(CRAs)和法规团队紧密合作,您将获得宝贵的临床研究流程经验,同时为有意义的医疗创新做出贡献。
职责

  • 维护和更新试验主文件(TMF)和研究文件
  • 支持文件准备、归档、跟踪和存档
  • 审核研究文件的完整性和合规性
  • 协调临床试验物资和跟踪记录
  • 协助CRF跟踪、研究问题和数据流程
  • 作为项目沟通和文件的关键联系人

您将带来的优势

  • 对临床研究和医疗保健的热情
  • 科学学位优先
  • 有行政、协调或医疗相关经验
  • 熟练使用Microsoft Office(Word、Excel、PowerPoint)
  • 强大的组织能力和细致入微的注意力
  • 能够管理多项任务并按时完成
  • 有效的沟通能力,能够在跨团队中协作工作

请注意:此职位不提供英国签证担保。

立即申请,开启一段更有意义的职业生涯,产生影响,并不断学习!
IQVIA是生命科学和医疗行业领先的临床研究服务、商业洞察和医疗智能提供商。我们创建智能连接,加速创新医疗治疗的开发和商业化,以帮助改善全球患者的预后和人群健康。了解更多信息,请访问
IQVIA致力于在招聘过程中保持诚信,对候选人欺诈采取零容忍政策。您提交的所有信息和资质必须真实完整。在招聘过程中任何虚假陈述、误导性信息或重要遗漏都将导致申请被立即取消,或在之后发现时终止雇佣,根据适用法律处理。我们感谢您的诚实和专业。

查看英文原文

Job Title: Clinical Trials Assistant II
Job Location: Reading, Berkshire, United Kingdom
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Join IQVIA on our mission to accelerate innovation for a healthier world!

As a Clinical Trials Assistant (CTA I OR CTA II), you'll support clinical studies by maintaining accurate documentation, coordinating study activities, and helping ensure projects stay compliant and on track. Working closely with Clinical Research Associates (CRAs) and Regulatory teams, you'll gain valuable exposure to the clinical research process while contributing to meaningful healthcare innovation.
Responsibilities

  • Maintain and update Trial Master Files (TMF) and study documentation
  • Support document preparation, filing, tracking, and archiving
  • Review study files for completeness and compliance
  • Coordinate clinical trial supplies and tracking records
  • Assist with CRF tracking, study queries, and data workflows
  • Act as a key contact for project communications and documentation

What You'll Bring

  • Passion for clinical research and healthcare
  • Science degree preferred
  • Previous administrative, coordination, or healthcare-related experience
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint)
  • Strong organisation skills and attention to detail
  • Ability to manage multiple priorities and meet deadlines
  • Effective communication skills with the ability to work collaboratively across teams

Please note: This role is not eligible for UK visa sponsorship.

Apply today and forge a career with greater purpose, make an impact, and never stop learning!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas

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