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Pfizer EG-Asso.I, SDMS in Wuhan, China


• 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.