Pharmacovigilance SME | Argus/Veeva | ₱30K Joining Bonus

Cognizant Technology Solutions Philippines Inc.; Taguig; On-site; PHP 312,000 - 469,000; Full time

Benefits offered by this job

Joining bonus ₱30,000*

Pioneer SME opportunity

Global exposure in drug safety

Job summary

Cognizant Technology Solutions Philippines Inc. is seeking a Pharmacovigilance Case Processing Associate (SME) to join our growing drug safety team in Manila.

You will process ICSRs, conduct AE intake and data entry, perform MedDRA and product coding, and help create safety narratives. This on-site role offers growth in global pharmacovigilance operations, opportunities to work with Argus and Veeva systems, and a chance to contribute to regulatory compliance while ensuring data integrity across

Qualifications

• 1–2 years pharmacovigilance experience.
• Experience with Argus Safety or Veeva Safety.
• Strong knowledge of MedDRA coding and AE reporting.
• Attention to data quality and narrative writing skills.

Responsibilities

• Process and review ICSRs
• Adverse event case intake and data entry
• MedDRA coding and product coding
• Create and maintain safety narratives
• Quality review and QC checks
• Manage safety workflows and case routing
• Ensure compliance with pharmacovigilance regulations
• Maintain data integrity in safety databases (Argus, Veeva)

Skills

Data entry

Narrative writing

Icsr management

MedDRA knowledge

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

Qualified hires may get a chance to win an iPhone 18 Pro Max through our FIRST WIN Promo.

Terms and conditions apply.*