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Pharmacovigilance Associate | Drug Safety | ICSR | Argus or Veeva Safety

Pharmacovigilance Associate | Drug Safety | ICSR | Argus or Veeva Safety

Cognizant Consulting
  • Posted 13 hours ago
  • Be among the first 10 applicants

Job Description

Job description

Cognizant is a global organization serving clients across multiple industries with a deep set of offerings provided by our practice areas and supported by corporate and enabling functions. Employing roughly 270,000 talented associates worldwide, Cognizant is dedicated to anticipating and solving clients toughest problems and enabling them to thrive in the digital era. Join us and Be Cognizant!

We are looking for a Pharmacovigilance Case Processing Associate to support the management of Individual Case Safety Reports (ICSRs) and ensure accurate safety data processing and regulatory compliance. This role is ideal for professionals with experience in Drug Safety, Pharmacovigilance, Case Processing, Argus Safety, Veeva Safety, MedDRA Coding, and Narrative Writing.

Key Responsibilities

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

Qualifications

Education

  • Bachelor's degree in Pharmacy or Nursing.
  • Professional license is an advantage but not required

Required Experience

  • 1-2 years of experience in Pharmacovigilance, Drug Safety, or ICSR Processing
  • Hands-on experience with Argus Safety, Veeva Safety, Oracle Argus, Safety Database Systems, or other PV platforms
  • Knowledge of:
  • Case Processing
  • Medical Coding / MedDRA Coding
  • Narrative Writing
  • Quality Review
  • Adverse Event Reporting
  • Strong English communication skills

Preferred Skills

  • ICSR Management
  • MedDRA Coding
  • WHO Drug Coding
  • Regulatory Reporting
  • Global Pharmacovigilance Operations
  • Clinical Research
  • Drug Safety Surveillance
  • Life Sciences Shared Services or Healthcare BPO experience

Why Join Us

At Cognizant, we don't just offer jobs—we build careers that thrive in the digital era.

  • Growth That Matters – Clear career paths, continuous learning, and opportunities to move into leadership or specialized roles. You're not just filling a seat—you're building a future.
  • Support That Empowers – A collaborative culture where your voice is heard, your ideas matter, and your well-being is prioritized through strong benefits and work-life balance.
  • Impact That Inspires – Work on global accounts that shape industries, influence millions of users, and give you a sense of purpose beyond the paycheck.

Your future starts here—grow, thrive, and make an impact with Cognizant.

More Info

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Key Skills

MedDRA Coding

Oracle Argus Safety Database Systems

Narrative Writing

ICSR Processing

Veeva Safety

Quality Review