Patient Safety Associate 患者安全专员

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As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than erapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Key Result Areas 主要领域 Safety report management 安全性报告管理
  • maintain and receive safety report from all in-take channels
维护和接收各渠道来源的安全性报告
  • Handle safety report from all sources (clinical studies, spontaneous, literatures, NMPA, etc.), including:
  • Data review, coding, translation and communication
  • Report to global Data entry site
  • Report to Health Authorities
  • Query answering
  • Tracking and archiving
  • Late case communication and complete CAPA
处理各种来源(包括临床研究、自发报告、文献、NMPA 反馈等)的安全性报告, 包括:
  • 数据审查、编码、翻译和交流
  • 报告至全球数据录入中心
  • 报告至当地监管机构
  • 解答质疑
  • 跟踪和存档
  • 沟通迟报案例并完成CAPA
  • QC peers and/or vendors case
检查来自其他同事和/或供应商报告的质量
  • Support team members and provide training to new staff
支持团队成员,为新员工提供培训 Other其他
  • Support or perform any other task that management deems appropriate.
支持或执行管理层认为适当的任何其他任务 Academic / Professional Qualification
  • Bachelors degree in medical, pharmacy or other relevant majors
医学、药学、或相关专业学士及以上
  • Familiar with PV laws and regulations, ensure the quality of various PV surveillance work
熟悉药物警戒法律法规,确保各项药物警戒工作质量
  • Familiar with GCP
熟悉GCP
  • Good organizational skills with the ability to multi-task and prioritize assignments (planning and organizing)
良好的组织能力,能够同时处理多项任务并确定任务的优先级(计划和组织)
  • Good verbal and written communication skills
良好的口头和书面沟通技巧
  • Good project management and problem solving skills
良好的项目管理和解决问题的能力
  • Proficient in common office software and office equipment operation skills
熟练掌握常用办公软件和办公设备操作技巧
  • At least 0-1 year working experience in Pharmacovigilance
0-1 年以上药物警戒相关工作经验

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.


Information :

  • Company : Fortrea
  • Position : Patient Safety Associate 患者安全专员
  • Location : 上海市
  • Country : CN

How to Submit an Application:

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Post Date : 2025-02-01 | Expired Date : 2025-03-03