1+ months

Safety Data Management Specialist

+ 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 appropriate workflow for case processing.

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

+ Write and edit 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.


Posted: 2019-09-12 Expires: 2019-11-13

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Safety Data Management Specialist


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