Pharmacovigilance Case Processing Associate (SME) | Argus/Veeva | ₱30,000 JB*

Private Advertiser; Taguig; On-site; PHP 312,000 - 402,000; Full time

Benefits offered by this job

Joining Bonus

Global exposure in Drug Safety

Career growth in Pharmacovigilance

Job summary

Private Advertiser is seeking a Pharmacovigilance Case Processing Associate (SME) to join our growing PV team, focusing on Argus and Veeva platforms.

You will process ICSRs, perform data entry and MedDRA coding, create safety narratives, and ensure quality across safety databases. A ₱30,000 joining bonus is offered with opportunities for global exposure and career growth in Drug Safety.

Qualifications

• 1–2 years Pharmacovigilance experience.
• Drug Safety or Case Processing experience.
• Experience using Argus Safety, Oracle Argus, Veeva Safety, or related safety systems.
• Knowledge of MedDRA, Narrative Writing, Adverse Event Reporting, Quality Review, ICSR Management.

Responsibilities

• Process and review Individual Case Safety Reports (ICSRs).
• Conduct adverse event case intake and data entry.
• Perform MedDRA coding and product coding activities.
• Create and maintain safety narratives.
• Complete quality review and quality control checks.
• Manage safety workflows and case routing.
• Ensure compliance with pharmacovigilance regulations.
• Maintain data integrity within Argus, Veeva, or similar safety databases.

Skills

MedDRA

Narrative Writing

Adverse Event Reporting

ICSR Management

Quality Review

Education

Pharmacy

Nursing

Medical Technology

Medical Laboratory Science

Biomedical Science

Molecular Biology

Pharmaceutical Chemistry

Tools

Argus Safety

Oracle Argus

Veeva Safety

Job description

Pharmacovigilance Case Processing Associate (SME) | Argus/Veeva

₱30,000 Joining Bonus*

Terms and conditions apply.

Join Our Growing Pharmacovigilance Team

Responsibilities

• Process and review Individual Case Safety Reports (ICSRs)

• Conduct adverse event case intake and data entry

• Perform MedDRA coding and product coding activities

• Create and maintain safety narratives

• Complete quality review and quality control checks

• Manage safety workflows and case routing

• Ensure compliance with pharmacovigilance regulations

• Maintain data integrity within Argus, Veeva, or similar safety databases

Requirements

Education

• Pharmacy

• Nursing

• Medical Technology

• Medical Laboratory Science

• Biomedical Science

• Molecular Biology

• Pharmaceutical Chemistry

Experience

• 1-2 years Pharmacovigilance experience

• Drug Safety or Case Processing experience

• Experience using Argus Safety, Oracle Argus, Veeva Safety, or related safety systems

• Knowledge of:

  • MedDRA

  • Narrative Writing

  • Adverse Event Reporting

  • Quality Review

  • ICSR Management

Preferred Background

• Global Pharmacovigilance Operations

• Regulatory Reporting

• WHO Drug Coding

• Clinical Research

• Healthcare BPO

• Life Sciences Shared Services

Benefits

₱30,000 Joining Bonus*

Opportunity to become a Pioneer SME

Global exposure in Drug Safety Operations

Career growth in Pharmacovigilance and Regulatory Compliance