INTERNSHIP DETAILS

Safety Operations Intern-DL 2027

CompanyIQVIA
LocationDalian
Work ModeOn Site
PostedApril 14, 2026
Internship Information
Core Responsibilities
The intern will assist in processing drug safety data, including tracking adverse events and managing project workflows. Responsibilities also include database entry, quality control, and the preparation of safety submission files.
Internship Type
part time
Company Size
77794
Visa Sponsorship
No
Language
Chinese
Working Hours
32 hours
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About The Company
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
About the Role
  • 工作职责
  • 协助主管处理药品不良反应安全数据，包括：收集和跟踪传入的不良事件（AE）/终点信息、确定传入事件的初始/更新状态、跟踪事件处理完成的时间表等工作。 协助主管管理项目工作流程，包括数据库录入、质量控制活动和药品安全数据报告的生成，准备药品安全提交档案等工作。 其他主管指派的协助任务等。
  • 任职要求

    通过日语N2检定，或具备同等程度日语能力；并通过大学英语CET4级或以上。

    学历要求为本科及以上，日语专业可，如具备生物、医药相关背景可优先考虑。

    能够保证每周至少出勤24-32小时。

  • 实习地点

  • 大连办公室：大连市高新园区腾飞软件园一期西翼10楼

    *接受远程和线下实习相结合的方式

  • 顺利通过实习期考核即可优先得到正式offer。

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 https://jobs.iqvia.com

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.

Key Skills
Japanese LanguageEnglish LanguageData EntryQuality ControlAdverse Event ReportingClinical ResearchSafety Data ManagementDocumentation
Categories
HealthcareScience & ResearchAdministrative