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Pe-Pharmacovigilance

0-2 years
Not Disclosed
10 Oct. 1, 2025
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

💊 Job Title: Pharmacovigilance Associate (PE)

Company: Cognizant
Employment Type: Full-time / Hybrid (Rotational shifts)
Location: Flexible / Hybrid
Job Function: Pharmacovigilance / Drug Safety / Life Sciences


🌍 About Cognizant

Cognizant is a global professional services company transforming clients’ business, operating, and technology models for the digital era. With over 300,000 associates worldwide, Cognizant fosters an inclusive, collaborative, and innovative work environment.
Learn more at 🔗 www.cognizant.com


🎯 Role Overview

As a Pharmacovigilance Associate, you will play a vital role in ensuring the safety and efficacy of pharmaceutical products. You will contribute to drug safety monitoring, case processing, and risk assessment, collaborating with cross-functional teams in a Pharma R&D context.


🧾 Key Responsibilities

Case Monitoring & Processing

  • Monitor and evaluate adverse event (AE) data to ensure drug safety and regulatory compliance

  • Conduct PV case processing and maintain accurate records of safety data

  • Assess clinical trial and post-marketing safety information for trends and risks

  • Perform initial research and analysis of safety data

Reporting & Documentation

  • Prepare and submit safety reports to regulatory authorities

  • Assist in the development of safety-related documents and reports

  • Ensure accurate documentation in PV databases and systems

  • Anonymize/redact source documents as required

Risk Management & Compliance

  • Support risk management strategies to mitigate identified safety risks

  • Ensure adherence to SOPs and regulatory guidelines

  • Contribute to process improvement initiatives in pharmacovigilance

Collaboration & Development

  • Work with cross-functional teams to ensure timely case resolution

  • Participate in ongoing training to stay updated on industry best practices

  • Support the implementation of new PV tools and technologies


🎓 Qualifications

  • Degree in Pharmacy, Life Sciences, or related scientific field

  • Strong analytical and problem-solving skills with attention to detail

  • Excellent communication and interpersonal skills

  • Proficiency in pharmacovigilance databases and software

  • Basic understanding of regulatory requirements and guidelines

  • Experience in PV Case Processing is a plus


🌟 Why Cognizant?

  • Join a high-caliber, collaborative team

  • Work in an inclusive and innovative environment

  • Opportunities for training, certification, and career growth

  • Global exposure in pharmacovigilance and life sciences projects


⚖️ Equal Opportunity Employer

Cognizant does not discriminate based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, veteran status, or other protected categories. Reasonable accommodations are available upon request: 📧 CareersNA2@cognizant.com


📝 Additional Information

  • Interviews may be in-person or virtual

  • Government-issued ID may be required during interviews

  • Compensation is subject to change in accordance with law