Asso I, Safety Assessment
4000-7000元
武漢洪山區(qū)
應(yīng)屆畢業(yè)生
學(xué)歷不限
武漢洪山區(qū)
應(yīng)屆畢業(yè)生
學(xué)歷不限
Asso I, Safety Assessment
4000-7000元
武漢洪山區(qū)
應(yīng)屆畢業(yè)生
學(xué)歷不限
武漢洪山區(qū)
應(yīng)屆畢業(yè)生
學(xué)歷不限
職位描述
該職位還未進(jìn)行加V認(rèn)證,請(qǐng)仔細(xì)了解后再進(jìn)行投遞!
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
工作地點(diǎn)
地址:武漢洪山區(qū)光谷生物城
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職位發(fā)布者
DAYA..HR
輝瑞(中國)研究開發(fā)有限公司

-
制藥·生物工程
-
1000人以上
-
中外合資(合資·合作)
-
浦東科苑路88號(hào)上海德國中心2幢501-533室
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