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Safety Data Analyst

1+ years
₹5–8 LPA
10 July 26, 2025
Job Description
Job Type: Full Time Education: BCS/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Safety Data Analyst | Baxter International Inc.
Location: Bengaluru, Karnataka
Work Mode: Full-time
Estimated Salary: ₹5–8 LPA (based on similar roles and industry standards)


About Baxter:
At Baxter, every role is united by a shared mission — to save and sustain lives. For over 85 years, Baxter’s medical innovations have transformed healthcare in hospitals, clinics, and homes across the globe. As a member of the Global Patient Safety (GPS) Data Management team, you’ll help uphold this mission by ensuring safety data integrity and regulatory compliance.


Role Overview:
The Safety Data Analyst I will support the generation of safety data reports, conduct database searches, and ensure accuracy and consistency in safety data reporting. This role requires collaboration with cross-functional stakeholders and plays a critical part in global patient safety data management.


Key Responsibilities:

  • Generate accurate periodic and ad-hoc safety reports from the pharmacovigilance database.

  • Develop and standardize SQL queries for consistency across reporting.

  • Interpret data requests accurately and collaborate with report requestors.

  • Act as a point of escalation for data integrity issues impacting global stakeholders.

  • Test and implement improvements in reporting systems in collaboration with IT and Safety Systems Analysts.

  • Use BI tools to develop new reporting formats.

  • Identify and address data inconsistencies, errors, or omissions.

  • Interface with cross-functional departments including Regulatory, Medical Affairs, Clinical, IT, and Quality.


Qualifications & Experience:

  • Education: Bachelor’s in Computer Science, Life Sciences, or related scientific discipline.

  • Experience:

    • 1+ year in safety data management or a similar domain.

    • Prior experience with SQL, MS Excel, and pharmacovigilance databases (e.g., ARISg).

    • Knowledge of PV terminology and experience with Business Intelligence tools (e.g., Business Objects) preferred.

  • Skills:

    • Strong analytical and troubleshooting capabilities.

    • Excellent organizational skills and attention to detail.

    • Strong written and verbal communication.

    • Ability to work collaboratively in a team and under strict timelines.


Why Join Baxter?

  • Be a part of a mission-driven company impacting millions globally.

  • Work in a collaborative, innovative environment.

  • Grow your skills in pharmacovigilance and data analytics.