Pharmacovigilance SME | Pharmacists, RNs, Life Science Graduates | ₱30K Bonus | Start ASAP

Cognizant; Taguig; On-site; PHP 350,000 - 550,000; Full time

Job summary

Cognizant Philippines is seeking a Pharmacovigilance Specialist to join our high-performing global drug safety team. You will process and review ICSRs, perform data entry, MedDRA coding, and safety narratives, while ensuring strict regulatory compliance.

The role emphasizes experience with Argus or Veeva safety databases and yields growth opportunities in pharmacovigilance and regulatory compliance. Global exposure and career progression are highlighted.

Qualifications

• 1–2 years Pharmacovigilance experience
• Experience with Argus Safety, Oracle Argus, Veeva Safety, or related safety systems
• MedDRA knowledge and narrative writing
• Icsr processing and quality control

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

Tools

Argus Safety

Veeva Safety

Safety databases

Job description

Ready to Start ASAP? Join Our Pharmacovigilance Team | Argus/Veeva |

Terms and conditions apply.

Join a high-performing global drug safety team and take the next step in your Pharmacovigilance career. We are actively hiring candidates who can start ASAP and have experience with Argus, Veeva, or similar safety databases.

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
• Life Sciences Shared Services

Opportunity to become a Pioneer SME

Global exposure in Drug Safety Operations

Career growth in Pharmacovigilance and Regulatory Compliance