Pharmacovigilance Specialist (Onsite Training; Hybrid 3x) - Taguig

Pharmacovigilance Specialist

Location: Taguig
Work Setup: Onsite during training; Hybrid after training (3 days onsite per week)
Start Date: November 3

Job Summary

We are looking for a Pharmacovigilance Specialist to support pharmacovigilance and drug safety operations, including safety case processing and validation using industry-standard safety databases.

Key Responsibilities

• Process and validate individual safety cases in accordance with pharmacovigilance procedures and regulatory requirements.

• Review, assess, and document adverse event and safety information accurately and within required timelines.

• Perform safety case processing using pharmacovigilance databases such as Veeva Safety and Argus.

• Ensure completeness, accuracy, and consistency of safety case data.

• Follow standard operating procedures, quality requirements, and applicable regulatory guidelines.

• Collaborate with internal teams to resolve case-related queries and ensure timely case completion.

• Maintain high standards of data quality, accuracy, and compliance.

Qualifications

• Pharmacy graduates are required; candidates with or without an active professional license may apply.

• Nursing graduates will also be considered.

• 1–2 years of experience in pharmacovigilance/safety case processing is preferred.

• Hands-on experience with Veeva Safety, Argus, or other pharmacovigilance safety databases is an advantage.

• Good written and verbal communication skills.

• Strong attention to detail and ability to work accurately with safety-related data.

• Willingness to work fully onsite during training and transition to a hybrid setup (3 days onsite per week) after moving to production.

• Must be willing to work in Taguig.

Recruitment Process

Validation (Talkpush) → Talkpush Exam → Virtual or Walk-in Interview