Pfizer Safety Data Management Specialist B.Pharm, M.Pharm,
Pharm. D, and Life Science Graduates
Primary 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 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
Education:
B.Pharm, M.Pharm, Pharm. D, and Life Science Graduates.
Post-graduation is an added advantage.
Experience:
Pharmacovigilance, Individual Case Safety Reports
processing. Knowledge of ARGUS database preferable. Min exp: 0 years Max exp:
1.5 year.
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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