Pharmacovigilance Specialist — Argus/Veeva Expert

Cognizant; Taguig; On-site; PHP 335,000 - 670,000; Full time

Job summary

Cognizant in the Philippines is seeking a Pharmacovigilance professional to join a global drug safety team. Start ASAP and work with Argus, Veeva, or similar safety databases to process ICSRs and ensure compliance.

Responsibilities include intake, data entry, MedDRA coding, safety narratives, quality checks, and case routing. Ideal candidates hold degrees in Pharmacy, Nursing, or Life Sciences, have PV experience, and are eager to grow in regulatory-compliance roles.

Qualifications

• 1-2 years pharmacovigilance experience.
• Experience using Argus Safety or Veeva Safety systems.
• Knowledge of MedDRA coding and ICSR handling.
• Narrative writing for safety reports and regulatory submissions.
• Quality review and data integrity checks in pharmacovigilance workflows.

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

ICSR Management

Narrative Writing

Adverse Event Reporting

Quality Review

MedDRA

Education

Pharmacy

Nursing

Medical Technology

Medical Laboratory Science

Biomedical Science

Molecular Biology

Pharmaceutical Chemistry

Tools

Argus Safety

Oracle Argus

Veeva Safety

Job description

Cognizant in the Philippines is seeking a Pharmacovigilance professional to join a global drug safety team. Start ASAP and work with Argus, Veeva, or similar safety databases to process ICSRs and ensure compliance.

Responsibilities include intake, data entry, MedDRA coding, safety narratives, quality checks, and case routing. Ideal candidates hold degrees in Pharmacy, Nursing, or Life Sciences, have PV experience, and are eager to grow in regulatory-compliance roles.