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# Global Pharmacovigilance Data Analyst

- **Company:** Baxter
- **Location:** Wien, Austria (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Clinical Data Management, Data Integrity, Database Queries, IBM Cognos Business Intelligence, SQL Databases, Sql Optimization, Information Technology, Data Analytics, Data Management, Tools for Reporting
- **Published:** September 29, 2026
- **Apply:** https://baxter.wd1.myworkdayjobs.com/baxter/job/Wien-Vienna/XMLNAME--Senior--Global-Pharmacovigilance-Data-Analyst--m-f-d-_JR-210392-1/apply

## About the Role

* Bachelor's degree in Computer Science, Information Technology, Data Analytics, Life Sciences or a related discipline.
 * Several years of experience in data analytics, reporting or database management.
 * Advanced SQL and database querying skills.
 * Strong experience investigating data quality and data integrity issues
 * Demonstrated ability to translate business requirements into scalable reporting solutions.
 * Excellent stakeholder management and communication skills.
 * Experience working in complex global and cross-functional environments.

Highly Desirable

 * Experience with Pharmacovigilance systems such as Argus or ARISg.
 * Experience with Cognos or comparable reporting platforms.
 * Pharmacovigilance, Drug Safety or Clinical Data Management experience
 * Experience with reporting automation and process improvement initiatives.

## Description

Do you enjoy solving complex data challenges and influencing global processes? Join Baxter's Global Pharmacovigilance Data Management team and take a leading role in ensuring the quality, reliability and accessibility of critical safety data across a global organization., As a Senior Global Pharmacovigilance Data Analyst (m/f/d) you will serve as a subject matter expert for pharmacovigilance reporting, data integrity and analytics. You will partner with global stakeholders, drive process improvements and help shape future reporting and automation capabilities within the organization., * Lead the development, validation and optimization of complex reporting solutions and SQL queries.

 * Generate and oversee critical periodic and ad hoc pharmacovigilance reports.
 * Act as an escalation point for complex data integrity and reporting issues. [Data
 * Conduct root cause analyses and drive sustainable corrective actions. [Data
 * Partner with IT, Safety Systems, Regulatory Affairs, Medical Affairs and other global functions.
 * Identify opportunities for automation and process optimization.
 * Support system enhancements, testing activities and implementation projects.
 * Mentor junior team members and share best practices across the organization.


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