艾昆纬
Safety Associate
Safety Associate
发布于 大约 16 小时前普通员工/个人贡献者
Taipei , Taipei City, Taiwan
初级经验
全职员工
仅现场办公
本科
医疗、制药与临床研究
Microsoft Office
Communication Skills
Attention To Detail
Clinical Research
AI 估算 · 8k–12k
Junior pharmacovigilance role in a global CRO, market rate for entry-level positions in Taiwan.
职位详情
关于这个职位
This role involves reviewing, assessing, and processing safety data from various sources, ensuring compliance with regulations and SOPs under the guidance of senior team members. It is a junior position in pharmacovigilance within a global clinical research organization.
最低要求
High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences Req
An Individual with a minimum of a Bachelor’s Degree in scientific or healthcare discipline or allied life sciences graduation with 1-1.5 years of relevant experience. Req
Good knowledge of medical terminology. Intermediate
Working knowledge of applicable Safety Database. Beginner
Knowledge of applicable global, regional, local clinical research regulatory requirements. Beginner
Excellent attention to detail and accuracy. Beginner
Good working knowledge of Microsoft Office and web-based applications. Beginner
Strong organizational skills and time management skills. Beginner
Strong verbal/written communication skills. Intermediate
Self-motivated and flexible. Intermediate
Ability to follow instructions/guidelines, utilize initiative and work independently. Intermediate
Ability to multi-task, manage competing priorities and deadlines. Beginner
Ability to delegate to less experienced team members. Beginner
Willingness and aptitude to learn new skills across Safety service lines. Beginner
Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients. Beginner
Ability to work as a Team Player, contribute and work towards achieving Team goals. Beginner
Ensure quality of deliverables according to the agreed terms. Beginner
Demonstration of IQVIA core values while doing daily tasks Beginner
Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Beginner
Regular sitting for extended periods of time. Beginner
May require occasional travel. Beginner
Flexibility to operate in shifts. Beginner
工作职责
To Prioritize and complete the assigned trainings on time.
Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
determining initial/update status of incoming events
database entry
coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.
Ensure to meet quality standards per project requirements.
Ensure to meet productivity and delivery standards per project requirements.
To ensure compliance to all project related processes and activities.
Creating, maintaining and tracking cases as applicable to the project plan.
Identify quality problems, if any, and bring them to the attention of a senior team member.
To demonstrate problem solving capabilities.
To mentor new teams members, if assigned by the Manager.
Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
% compliance towards all people practices and processes
Perform other duties as assigned.
AI 洞察
优缺点分析
优点
- Work at a leading global CRO with robust training and career development opportunities.
- Gain hands-on experience in pharmacovigilance, a critical and growing field in healthcare.
- Collaborate with diverse teams and gain exposure to international regulatory standards.
- High attention to detail is required, with strict timelines and quality standards.
- Shift flexibility may be needed, and the role involves repetitive data entry tasks.
- Limited autonomy initially, with close guidance from senior team members.
- This role is ideal for graduates in life sciences who are detail-oriented, eager to learn, and interested in starting a career in drug safety and clinical research.
缺点 / 挑战
暂无明显挑战项
角色解读
- Progress within pharmacovigilance to roles such as Senior Safety Associate or Team Lead.
- Move into broader drug safety or regulatory affairs functions within the pharmaceutical industry.
- Develop expertise in specific therapeutic areas or advanced safety analytics.
- Process and manage adverse event reports from various sources, ensuring timely and accurate data entry and case processing.
- Perform pharmacovigilance activities such as coding medical terms, writing narratives, and conducting literature reviews.
- Maintain compliance with global and local regulations, SOPs, and project-specific requirements.
- Strong foundation in medical terminology and clinical research processes.
- Proficiency in using safety databases and Microsoft Office tools.
- Excellent attention to detail and ability to handle multiple priorities under deadlines.
申请策略
- Tailor your resume to reflect compliance and quality focus, as the role prioritizes accuracy.
- Research IQVIA's values and recent projects to demonstrate genuine interest.
- Emphasize any academic or internship experience in pharmacovigilance, clinical research, or healthcare.
- Highlight proficiency in medical terminology and data management tools.
- Showcase organizational skills and ability to work in a team-oriented environment.
- Familiarize yourself with common safety databases (e.g., Argus, ARISg) and regulatory guidelines (ICH-GCP).
- Practice attention to detail through case studies or mock data entry exercises.
- Improve communication skills for clear reporting and collaboration.
面试指南
- For process questions, use the STAR method (Situation, Task, Action, Result) to structure your response.
- For technical knowledge, demonstrate understanding of AE reporting and regulatory requirements.
- For behavioral questions, provide concrete examples that highlight your organizational and communication skills.
- What is your understanding of pharmacovigilance and its importance in drug development?
- Describe a time when you had to handle multiple tasks under strict deadlines.
- How do you ensure accuracy and attention to detail in your work?
- Are you comfortable working in shifts and occasionally traveling?
- Review basic pharmacovigilance concepts, including adverse event coding and regulatory timelines.
匹配度报告
69
综合匹配度
Entry-level pharmacovigilance role at a global CRO, offering solid training and purpose but with shift work and limited flexibility.
适合人群
This role is best suited for candidates who prioritize meaningful work in healthcare and career development over work-life balance and high initial compensation.
最强匹配
使命价值匹配
最弱匹配
工作生活匹配
薪资福利65
成长发展75
工作生活55
使命价值80
薪资福利匹配
65中等
The salary range is competitive for entry-level in Taiwan but not exceptionally high; includes standard benefits but no explicit mention of bonuses or perks.
薪资信号面议 (8K-12K/月)
成长发展匹配
75中等
The role offers good on-the-job training and growth into senior positions, with exposure to global regulatory practices.
技术前沿传统/成熟技术
技术栈Safety Database、Microsoft Office
成长机会mentor new teams members、trainings
业务类型ambiguous
工作生活匹配
55较低
Requires shift work and occasional travel; limited flexibility; office-based role without remote options.
工作模式仅现场办公
办公地点未明确
加班情况JD含高强度暗示词
使命价值匹配
80较高
The role contributes to patient safety and drug development, with a strong sense of purpose in healthcare.
行业发展稳定成熟行业
社会影响正向社会影响力较高
使命信号improve patient outcomes
创新程度稳健跟随主流
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