Pharmacovigilance Specialist (Taguig) | Hybrid

Work Setup: Willing to work full onsite during training and hybrid (3x onsite per week) upon production in Taguig

Work Schedule: Night shift

Start Date: Nov 3, 2026

Requirements:

• 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:

• 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.