Associate Manager Clinical Data Sciences
9000元以上
應(yīng)屆畢業(yè)生
學(xué)歷不限



- 全勤獎(jiǎng)
- 節(jié)日福利
- 不加班
- 周末雙休
職位描述
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ROLE SUMMARY02
As part of the Clinical Data Sciences group, an integral delivery unit within
the Global Biometrics and Data Management (GBDM) organization, the Associate
Manager,Central Monitor (CM), Data Surveillance is responsible for timely and
high quality risk-based monitoring analytics supporting the Pfizer portfolio
withminimum supervision. The Associate Manager, Central Monitor, Data
Surveillance will support an approach to clinical trial monitoring which
utilizes data and site level information to determine needs for performing
on-site,remote and centralized activities and focuses resources on risks that
have the most potential toimpact patients’ safety and data quality, with
supervision.02
02
ROLE RESPONSIBILITIES0202
General:02
*
Implement global strategies, initiatives, processes, and standards to ensure
consistent, efficient, and quality processes to meet quality,timelines and
deliverables.02
*
Provide technical expertise to set up and test study level Risk-based
Monitoringsystem02
*
Review study level system outputs to process for the signal and action
management02
*
Plan and execute communication plans
As part of the Clinical Data Sciences group, an integral delivery unit within
the Global Biometrics and Data Management (GBDM) organization, the Associate
Manager,Central Monitor (CM), Data Surveillance is responsible for timely and
high quality risk-based monitoring analytics supporting the Pfizer portfolio
withminimum supervision. The Associate Manager, Central Monitor, Data
Surveillance will support an approach to clinical trial monitoring which
utilizes data and site level information to determine needs for performing
on-site,remote and centralized activities and focuses resources on risks that
have the most potential toimpact patients’ safety and data quality, with
supervision.02
02
ROLE RESPONSIBILITIES0202
General:02
*
Implement global strategies, initiatives, processes, and standards to ensure
consistent, efficient, and quality processes to meet quality,timelines and
deliverables.02
*
Provide technical expertise to set up and test study level Risk-based
Monitoringsystem02
*
Review study level system outputs to process for the signal and action
management02
*
Plan and execute communication plans
工作地點(diǎn)
地址:武漢洪山區(qū)光谷生物城
查看地圖


職位發(fā)布者
車艷鑫HR
輝瑞(中國(guó))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)
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浦東科苑路88號(hào)上海德國(guó)中心2幢501-533室
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