Pharmacovigilance SME — Global Drug Safety Expert

Cognizant

Taguig

On-site

PHP 391,000 - 614,000

Full time

2 days ago

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Benefits offered by this job

₱30,000 Joining Bonus*

Job summary

Cognizant is seeking a Pharmacovigilance Case Processing Associate to join our pioneering pharmacovigilance practice. You will handle ICSR processing, data entry, and safety narrative preparation, using Argus Safety, Veeva Safety, MedDRA coding, and related PV platforms to ensure high-quality case management.

The role requires 1–2 years in pharmacovigilance, with bachelor's degrees in life sciences or healthcare fields preferred.

Qualifications

1–2 years of experience in Pharmacovigilance, Drug Safety, or ICSR Processing.
Experience with Argus Safety, Veeva Safety, Oracle Argus, Safety Database Systems, or other PV platforms.

Responsibilities

Process and manage Individual Case Safety Reports (ICSRs)
Perform case intake, data entry, and case book-in activities
Prepare and update safety case narratives
Utilize MedDRA and product coding
Perform quality reviews and case assessments
Manage workflow updates, case routing, and case closure
Support labeling and regulatory compliance activities
Ensure timely reconciliation and submission readiness
Maintain data accuracy within pharmacovigilance safety databases

Skills

Drug Safety

ICSR Processing

Argus Safety

Veeva Safety

MedDRA Coding

Narrative Writing

Education

Bachelor's Degree in Pharmacy, Nursing, Medical Technology/Medical Laboratory Science, Biomedical Science, Molecular Biology, or Pharmaceutical Chemistry