艾昆纬
Clinical Trials Assistant (CTA)
Clinical Trials Assistant (CTA)
发布于 大约 4 小时前普通员工/个人贡献者
Taipei , Taipei City, Taiwan
中级经验
全职员工
仅现场办公
高中/中专
医疗、制药与临床研究
Microsoft Office
ICH
Regulatory
Clinical Research
AI 估算 · 6k–9k
临床助理岗位，经验要求3年，跨国CRO公司，薪资在台北属中等水平。
职位详情
关于这个职位
This role is a Clinical Trials Assistant (CTA) at IQVIA, supporting clinical research operations. You will assist Clinical Research Associates and Regulatory teams with document management, trial master file maintenance, and administrative tasks to ensure compliance with GCP and ICH guidelines. The position is based in Taipei, Taiwan and offers exposure to global clinical trials.
最低要求
High School Diploma or equivalent required.
years of administrative support experience.
Equivalent combination of education, training and experience.
Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
Written and verbal communication skills including good command of English language.
Effective time management and organizational skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
Knowledge of applicable protocol requirements as provided in company training.
工作职责
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
Assist with periodic review of study files for completeness.
Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
AI 洞察
优缺点分析
优点
- Entry point into clinical research industry at a top global CRO.
- Exposure to full clinical trial lifecycle and regulatory requirements.
- Opportunity to work with experienced CRAs and gain hands-on site monitoring experience.
- Good foundation for career growth into higher clinical roles.
- Highly administrative and documentation-focused work may be repetitive.
- Requires meticulous attention to detail and ability to manage multiple tasks.
- Limited autonomy initially
- work is closely supervised.
- This role is ideal for individuals with administrative experience looking to break into clinical research. It suits detail-oriented, organized candidates who are comfortable with routine tasks and eager to learn about clinical trials.
缺点 / 挑战
暂无明显挑战项
角色解读
- Progress to Clinical Research Associate (CRA) with experience and further training.
- Move into regulatory affairs or clinical project management roles.
- Gain expertise in clinical operations and specialize in therapeutic areas.
- Maintain and update clinical trial documentation and systems like Trial Master File (TMF).
- Assist CRAs and regulatory teams with preparing, handling, and distributing clinical supplies and reports.
- Track and manage case report forms, queries, and clinical data flow.
- Act as a central contact for project communications and may accompany CRAs on site visits.
- Strong organizational and time management skills to manage multiple documents and deadlines.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint) for documentation and tracking.
- Good command of English for communication and understanding of clinical protocols.
- Awareness of GCP and ICH guidelines to ensure compliance.
申请策略
- Tailor your cover letter to express interest in clinical trials and IQVIA’s global impact.
- Be prepared to discuss your organizational methods and experience with documentation.
- Emphasize administrative support experience, especially in regulated environments.
- Highlight any familiarity with clinical research or healthcare settings.
- Showcase proficiency in Microsoft Office and organizational achievements.
- Demonstrate English language skills if not native.
- Learn about GCP and ICH guidelines through online courses (e.g., CITI Program).
- Practice using document management systems and Excel for data tracking.
面试指南
- Use STAR method (Situation, Task, Action, Result) for behavioral questions.
- For knowledge questions, show awareness and willingness to learn
- reference company training.
- Focus on transferable skills: organization, attention to detail, communication.
- What do you know about GCP and why is it important in clinical trials?
- Describe your experience with maintaining files or tracking documents in a previous role.
- How do you prioritize tasks when dealing with multiple deadlines?
- Give an example of a time you had to communicate complex information clearly.
职位点评
64
综合评分
Stable CRO role with clear growth path, moderate pay, office-based in Taipei.
更适合这类人
This position is best for candidates prioritizing career growth in clinical research over high compensation or flexible work arrangements.
表现最好
成长发展
相对薄弱
工作生活
薪资福利60
成长发展75
工作生活50
使命价值70
薪资福利
60中等
Salary is competitive for Taiwan but not high for the industry; benefits not specified. Overall moderate compensation.
薪资信号未披露（AI估算：6K-9K/月）
成长发展
75中等
Good entry point for clinical research career with clear growth path to CRA; training provided but not explicitly mentioned.
技术前沿传统/成熟技术
技术栈GCP、ICH、TMF、Microsoft Office
成长机会May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training
业务类型cost_center
工作生活
50较低
Office-based work in Taipei; no mention of flexibility or WLB. Likely standard hours but may involve site visits.
工作模式仅现场办公
办公地点市区核心地段
加班情况未提及（无法判断）
使命价值
70中等
Working in clinical research contributes to improving patient health; however role is administrative and not directly involved in patient care.
行业发展稳定成熟行业
社会影响中性/一般
使命信号accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes
创新程度稳健跟随主流
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