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Safety Data Management Specialist (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
REFERENZNUMMER:
334114/11
IHRE AUFGABEN:
-Carry out case processing activities of adverse events/adverse drug reactions
-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
IHRE QUALIFIKATIONEN:
-Professional in health care (e.g. nurse) or equivalent experience preferred
-Experience in pharmacovigilance and/or data management, clinical care or clinical/scientific research preferred but not required
-Experience in use and management of relational databases preferred
-Good knowledge in medical terminology
-Ability to solve routine problems under supervision and to surface issues constructively
-Ability to make basic decisions with an understanding of the consequences
-Fluency in spoken and written English and German
-Good understanding of written French
-Good understanding of written Italian is an advantage
WEITERE QUALIFIKATIONEN:
Drug safety manager
334114/11
IHRE AUFGABEN:
-Carry out case processing activities of adverse events/adverse drug reactions
-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
IHRE QUALIFIKATIONEN:
-Professional in health care (e.g. nurse) or equivalent experience preferred
-Experience in pharmacovigilance and/or data management, clinical care or clinical/scientific research preferred but not required
-Experience in use and management of relational databases preferred
-Good knowledge in medical terminology
-Ability to solve routine problems under supervision and to surface issues constructively
-Ability to make basic decisions with an understanding of the consequences
-Fluency in spoken and written English and German
-Good understanding of written French
-Good understanding of written Italian is an advantage
WEITERE QUALIFIKATIONEN:
Drug safety manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges