應(yīng)屆畢業(yè)生
學(xué)歷不限
最近更新
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職位描述
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工作職責(zé): ROLE SUMMARY The Central Monitor II is responsible for ensuring the
completeness, quality and integrity of the subject data in the clinical trial
database under Risk Based Monitoring (RBM) mode. The areas of activity include
but are not limited to: developing Risk-Based Monitoring system for applicable
studies, ensuring key risk indicators (KRIs) properly defined and set up in the
system to support the study, processing and reviewing study data in the system
for the signal and action management, follow up for the issue resolution. The
Central Monitor I ensures risk based monitoring activities comply with
regulations, applicable Standard Operating Procedures (SOPs) and Processes at
all times and is familiar with supported systems (RBM system, etc.) and able to
troubleshoot and provide rapid response for all database issues. The Central
Monitor I works with the global study team to meet the study objectives. ROLE
RESPONSIBILITIES General: Implement global strategies, initiatives, processes,
and standards to ensure consistent, efficient, and quality processes to meet
quality, timelines and deliverables. Provide technical expertise to set up and
test study level Risk-based Monitoring system Review study level system outputs
to process for the signal and action management Execute communication plans
completeness, quality and integrity of the subject data in the clinical trial
database under Risk Based Monitoring (RBM) mode. The areas of activity include
but are not limited to: developing Risk-Based Monitoring system for applicable
studies, ensuring key risk indicators (KRIs) properly defined and set up in the
system to support the study, processing and reviewing study data in the system
for the signal and action management, follow up for the issue resolution. The
Central Monitor I ensures risk based monitoring activities comply with
regulations, applicable Standard Operating Procedures (SOPs) and Processes at
all times and is familiar with supported systems (RBM system, etc.) and able to
troubleshoot and provide rapid response for all database issues. The Central
Monitor I works with the global study team to meet the study objectives. ROLE
RESPONSIBILITIES General: Implement global strategies, initiatives, processes,
and standards to ensure consistent, efficient, and quality processes to meet
quality, timelines and deliverables. Provide technical expertise to set up and
test study level Risk-based Monitoring system Review study level system outputs
to process for the signal and action management Execute communication plans
注：聯(lián)系我時，請說是在浦口人才網(wǎng)上看到的。
工作地點
地址：雞西密山市輝瑞（中國）研究開發(fā)有限中心
求職提示：用人單位發(fā)布虛假招聘信息，或以任何名義向求職者收取財物（如體檢費、置裝費、押金、服裝費、培訓(xùn)費、身份證、畢業(yè)證等），均涉嫌違法，請求職者務(wù)必提高警惕。
職位發(fā)布者
車艷鑫HR
輝瑞(中國)研究開發(fā)有限公司
-
制藥·生物工程
-
1000人以上
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中外合資（合資·合作）
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浦東科苑路88號上海德國中心2幢501－533室
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