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Associate I, Safety Data Management Specialist

Pfizer


Location:
Wuhan R&d Center
Date:
01/26/2018
2018-01-262018-03-02
Pfizer
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Job Details

Responsibilities



Carry out case processing activities



Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments



Review case criteria to determine the appropriate workflow for case processing



Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately



Write and edit the case narrative



Determine and perform appropriate case follow-up, including generation of follow-up requests



Review processed cases to verify accuracy, consistency, and compliance with process requirements, and review case data for special scenarios



Liaise with key partners, locally , and other stakeholders regarding safety data collection and data reconciliation



Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database



Determine reportability of scheduled reports , ensuring adherence to regulatory requirements



Consistently apply regulatory requirements and Pfizer policies



Participate, as appropriate, in local, internal and external safety activities







Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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