Associate II, Safety Data Management Specialist
7-9千
 武汉-东湖新技术产业开发区
 无需经验
 本科
 全职
 更新于05-15
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职位信息

Use Your Power for Purpose
At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will Achieve
In this role, you will:
● Monitor the company's drug, biologics, and medical devices surveillance program.
● Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities.
● Make decisions within limited options to resolve problems, under the supervisor's direction.
● Work in a structured environment, following established procedures.
● Ensure work is regularly reviewed for technical judgment, completeness, and accuracy.
● Provide expertise on regulatory requirements and corporate policies for regulatory submissions to project teams.
● Support Worldwide Strategy and Regulatory teams by analyzing post-marketing safety data, reviewing medical literature, and related activities.
● Determine the appropriate workflow for case processing by reviewing case criteria.
Here Is What You Need (Minimum Requirements):
● BA/BS with any years of experience
● Strong analytical skills with the ability to interpret complex data
● Proficiency in using safety databases and software
● Excellent written and verbal communication skills
● Ability to work collaboratively in a team environment
● Basic understanding of regulatory requirements and corporate policies
Bonus Points If You Have (Preferred Requirements):
● Experience in pharmacovigilance or drug safety
● Familiarity with medical terminology and coding systems
● Knowledge of global regulatory requirements for drug safety
● Strong problem-solving skills and the ability to make decisions with limited information
● Proficiency in multiple programming languages and frameworks
● Experience with cloud platforms and services
● Familiarity with agile methodologies and project management tools
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE
工作地址
 辉瑞(武汉)研究开发有限公司
应届生安全提醒
求职过程中如果遇到违规收费、信息不实、以招聘名义的培训收费或者微信营销等虚假招聘行为,请保留证据,维护自己的合法权益。谨防上当受骗!
公司信息
On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards.
辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外,该中心是辉瑞全球安全和风险管理部的一个分支,负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。
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img辉瑞(中国)研究开发有限公司
外资(欧美)
10000人以上
制药/生物工程
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