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Baxter is hiring a PV Specialist (Pharmacovigilance Specialist) for its Global Patient Safety (GPS) team in Gurgaon, Haryana. If you have strong skills in ICSR processing, narrative writing, MedDRA coding, and pharmacovigilance regulations, this is an excellent opportunity to build your career with a leading global healthcare company.
This job focuses on individual case safety report processing, ensuring high-quality adverse event (AE) documentation, and supporting Baxter’s mission to save and sustain lives.
Key Responsibilities
As a PV Specialist, you will be responsible for:
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- Processing adverse event reports from all reporting sources
- Performing review and complete data entry for AE cases
- Determining seriousness, expectedness, causality, and medical assessment
- Ensuring accurate suspect drug selection in the PV safety database
- Writing high-quality medical narratives
- Coding medical terms using MedDRA and other standardized dictionaries
- Ensuring complete and accurate data coding and case integrity
- Coordinating with global/local affiliates for follow-up and case investigations
- Performing quality checks and case clean-up for aggregate reporting
- Working under timelines with high attention to detail and compliance standards
Required Qualifications
- Degree in Nursing, Pharmacy, Life Sciences, or relevant scientific discipline
- 2–3 years of experience in hospital care, pharmaceutical safety, or regulatory roles (preferred)
- Strong medical and clinical knowledge
- Excellent written and verbal communication
- Familiarity with global pharmacovigilance regulations
- Ability to work both independently and in a team
- Experience with Pharmacovigilance Safety Systems (preferred)
Job Benefits
Working at Baxter provides:
- Opportunity to contribute to global patient safety initiatives
- Inclusive, diverse, and collaborative work culture
- Competitive salary package
- Career growth in a global healthcare leader
- Exposure to advanced Pharmacovigilance systems and global processes
How to Apply

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