Pharmacovigilance Specialist (Taguig) | Hybrid

Philippines·TaguigFull-timemid

Laboratory & Life SciencesPharmacovigilance Specialist

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Quick Summary

Key Responsibilities

Perform case processing activities, including book-in, data entry, narrative writing (I-Narrative), and medical/product coding. Conduct quality checks using online QC tools,

Requirements Summary

Educational Attainment - Graduate of any of the following courses: BS Medical Technology / Medical Laboratory Science, BS Biomedical Science, BS Molecular Biology, BS Pharmaceutical Chemistry,

Technical Tools

Laboratory & Life SciencesPharmacovigilance Specialist

Requirements

~1 min read

Educational Attainment - Graduate of any of the following courses: BS Medical Technology / Medical Laboratory Science, BS Biomedical Science, BS Molecular Biology, BS Pharmaceutical Chemistry, BS Nursing, BS Pharmacy

1 to 2 years of safety case processing experience in Pharmacovigilance Safety databases: Argus OR Veeva Vault Safety or LSMV / Arisg or any other Pharmacovigilance safety database
Good communication skills
Willing to work full onsite during training and hybrid (3x onsite per week) upon production in Taguig

Responsibilities

~1 min read

→Perform case processing activities, including book-in, data entry, narrative writing (I-Narrative), and medical/product coding.
→Conduct quality checks using online QC tools, perform un-blinding (when required), and ensure completeness and accuracy of case documentation.
→Manage end-to-end case workflow, including case routing, case closure/lock, and labeling activities, including USPI labeling, in compliance with established procedures and timelines.