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Spec, Pv

2-3 years
Not Disclosed
10 Dec. 9, 2025
Job Description
Job Type: Full Time 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

Specialist, Pharmacovigilance (PV)

Job ID: JR-193249
Location: Gurgaon, Haryana, India
Category: Patient Safety
Posted on: December 3, 2025

Overview

Baxter is a global healthcare leader committed to enabling access to safe and effective care. Since 1931, the company has focused on advancing patient well-being and improving healthcare delivery worldwide. This role offers the opportunity to contribute directly to patient safety while being part of a collaborative, mission-driven organization dedicated to saving and sustaining lives.

Position Summary

The Specialist, Pharmacovigilance (PV) is a key member of the Global Patient Safety (GPS) Safety Operations team. The role is responsible for individual case safety report (ICSR) processing, ensuring accurate assessment, review, and timely reporting of adverse events across global markets.

This position requires strong medical judgment, understanding of worldwide safety regulations, and the ability to manage multiple priorities within strict timelines.

Key Responsibilities

  • Process adverse event reports from all data sources, including full medical review and detailed data entry.

  • Assess seriousness, expectedness, causality, and clinical outcome of each reported event.

  • Ensure accurate identification and selection of suspect products within the Pharmacovigilance Safety System.

  • Prepare clear and medically accurate case narratives.

  • Code clinical terms using MedDRA and ensure consistency across all safety data.

  • Verify all case information and ensure data quality before reporting.

  • Conduct follow-ups, generate queries, and request additional information from reporters and affiliate partners.

  • Perform quality checks and case clean-up activities as needed for aggregate reporting.

Required Qualifications

  • Strong medical and clinical knowledge.

  • Excellent written and verbal communication skills.

  • Ability to work independently under deadlines and adapt to shifting priorities.

  • Effective team collaboration skills.

  • Working knowledge of global and regional pharmacovigilance regulations.

  • Proficiency or ability to gain proficiency in Pharmacovigilance Safety Systems and safety databases.

Education and Experience

  • Degree in Nursing, Pharmacy, Life Sciences, or an equivalent scientific discipline.

  • Experience in the pharmaceutical industry (Regulatory Affairs or Pharmacovigilance) is preferred.

  • Minimum 2 to 3 years of hospital, clinical, or patient care experience preferred.

Equal Opportunity Commitment

Baxter is an equal opportunity employer and evaluates all applicants without discrimination based on race, color, religion, gender, national origin, age, disability, sexual orientation, gender identity, or veteran status.

Accessibility and Accommodation

Baxter provides reasonable accommodations for applicants with disabilities. Candidates requiring assistance during the application or interview process may request support by contacting the company with details of their requirements.

Recruitment Fraud Notice

Applicants are advised to stay aware of recruitment scams involving individuals falsely claiming affiliation with Baxter. Review the official Recruitment Fraud Notice to understand how to protect your personal information.

Work Location

Baxter (India) Pvt. Ltd
5th Floor, Tower A, Building No. 9
DLF Cyber City, DLF Phase III
Gurgaon – 122002, Haryana, India