Pfizer is seeking a Safety Data Management Specialist in Buenos Aires, Argentina, responsible for reviewing and processing adverse drug experience reports to ensure compliance with regulatory requirements. The ideal candidate should possess relevant experience or education in healthcare, strong analytical skills, and fluency in English
Job Summary
Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency.
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.
Consistently apply regulatory requirements and Pfizer policies.
Matching Summary
Match Score: 75
Pfizer is seeking a Safety Data Management Specialist in Buenos Aires, Argentina, responsible for reviewing and processing adverse drug experience reports to ensure compliance with regulatory requirements. The ideal candidate should possess relevant experience or education in healthcare, strong analytical skills, and fluency in English.
Skills & Requirements
Must-have
case processing activities
safety data collection
regulatory requirements
Pfizer policies
safety database
Nice-to-have
medical writing skills
problem solving
constructive issue surfacing
Key Requirements
Health Care Professional or equivalent experience preferred