[한국화이자제약] Drug Safety Unit - Safety Data Management Specialist
한국화이자제약
Hybrid
Adverse drug experience reporting
Safety data collection
Regulatory compliance
Pfizer is seeking a Safety Data Management Specialist to join their Drug Safety Unit, focusing on the review and reporting of adverse drug experiences. The ideal candidate should have a Bachelor's degree, fluency in Korean and English, and preferably some experience in pharmacovigilance or data management
Job Summary
Review, preparation, and completion of reports of adverse drug experiences to determine the safety profile of Pfizer’s products and to meet regulatory requirements.
Carry out case processing activities including reviewing, ranking, verifying, processing, and documenting case-related information.
Develop and maintain expertise and knowledge for applicable corporate and global regulations, guidelines, Standard Operating Procedures, data entry conventions, and search functions in the safety database.
Matching Summary
Match Score: 80
Pfizer is seeking a Safety Data Management Specialist to join their Drug Safety Unit, focusing on the review and reporting of adverse drug experiences. The ideal candidate should have a Bachelor's degree, fluency in Korean and English, and preferably some experience in pharmacovigilance or data management.
Skills & Requirements
Must-have
Adverse drug experience reporting
Safety data collection
Regulatory compliance
Pharmacovigilance database management
Korean and English fluency
Nice-to-have
Medical writing skills
Problem-solving abilities
Team collaboration
Adaptability to regulations
Key Requirements
Bachelor's Degree
Fluency in Korean & English
Healthcare Professional or equivalent experience preferred
1-2 years of experience in pharmacovigilance or clinical research preferred