职位描述
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Position Purpose
· Review, preparation, and completion of reports of adverse drug experiences,
to determine the safety profile of Pfizer’s products and to meet regulatory
requirements.
Primary Responsibilities
· Identify and select routine cases for processing, determining appropriate
prioritization criteria, and noting reasons for any delays.
· Assess cases to distinguish those with particular complexities and/or
specific issues, and escalate appropriately.
· Review, rank, verify, process and document: event terms; case
classifications (validity, seriousness,expectedness/listedness/labeledness);
special scenarios; product complaint information; reportability with due date;
and accuracy and consistency. Based on assessment of cases, process accordingly.
· Review case criteria to determine the appropriate workflow for case
processing.
· Write and edit the case narrative.
· Generate reports, ensuring adherence to regulatory compliance timelines.
· Determine appropriate case follow-up, requesting follow-up letters when
appropriate.
· Liaise with key partners, including Pfizer Country Organizations, Clinical
Development, License Partners, and other stakeholders regarding safety data
collection and data reconciliation.
· Develop and maintain expertise and knowledge of all products within the
Pfizer portfolio; applicable corporate and global regulations, guidelines,
Standard Operating Procedures and writing practices; data entry conventions;
and search functions in the safety database.
· Consistently apply regulatory requirements and Pfizer policies.
Technical Skill Requirements
· Experience in pharmacovigilance, in clinical care, or in clinical or
scientific research is an advantage but not a requirement.
· Demonstrated computer literacy, particularly in the use and management of
relational databases.
· Ability to achieve personal objectives while meeting departmental standards
of performance.
· Ability to work under supervision in a matrix organization.
· Excellent oral and written communication skills.
· Fluency in spoken and written English; knowledge of additional language(s)
an advantage.
· Experience and skill with medical writing an advantage.
Qualifications (i.e., preferred education, experience, attributes)
· Ability, with supervision, to solve routine problems and to surface issues
constructively.
· Ability to make basic decisions with an understanding of the consequences.
· Bachelor’s degree in a science-related field, pharmacy, nursing, or
equivalent; healthcare professional qualification preferred.
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
· Review, preparation, and completion of reports of adverse drug experiences,
to determine the safety profile of Pfizer’s products and to meet regulatory
requirements.
Primary Responsibilities
· Identify and select routine cases for processing, determining appropriate
prioritization criteria, and noting reasons for any delays.
· Assess cases to distinguish those with particular complexities and/or
specific issues, and escalate appropriately.
· Review, rank, verify, process and document: event terms; case
classifications (validity, seriousness,expectedness/listedness/labeledness);
special scenarios; product complaint information; reportability with due date;
and accuracy and consistency. Based on assessment of cases, process accordingly.
· Review case criteria to determine the appropriate workflow for case
processing.
· Write and edit the case narrative.
· Generate reports, ensuring adherence to regulatory compliance timelines.
· Determine appropriate case follow-up, requesting follow-up letters when
appropriate.
· Liaise with key partners, including Pfizer Country Organizations, Clinical
Development, License Partners, and other stakeholders regarding safety data
collection and data reconciliation.
· Develop and maintain expertise and knowledge of all products within the
Pfizer portfolio; applicable corporate and global regulations, guidelines,
Standard Operating Procedures and writing practices; data entry conventions;
and search functions in the safety database.
· Consistently apply regulatory requirements and Pfizer policies.
Technical Skill Requirements
· Experience in pharmacovigilance, in clinical care, or in clinical or
scientific research is an advantage but not a requirement.
· Demonstrated computer literacy, particularly in the use and management of
relational databases.
· Ability to achieve personal objectives while meeting departmental standards
of performance.
· Ability to work under supervision in a matrix organization.
· Excellent oral and written communication skills.
· Fluency in spoken and written English; knowledge of additional language(s)
an advantage.
· Experience and skill with medical writing an advantage.
Qualifications (i.e., preferred education, experience, attributes)
· Ability, with supervision, to solve routine problems and to surface issues
constructively.
· Ability to make basic decisions with an understanding of the consequences.
· Bachelor’s degree in a science-related field, pharmacy, nursing, or
equivalent; healthcare professional qualification preferred.
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
工作地点
地址:武汉洪山区光谷生物城
查看地图
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职位发布者
车艳鑫HR
辉瑞(中国)研究开发有限公司
![](http://img.jrzp.com/jrzpfile/provincercw/images/sfrz_yrz.png)
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制药·生物工程
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1000人以上
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中外合资(合资·合作)
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浦东科苑路88号上海德国中心2幢501-533室