Global Pharmacovigilance Data Analyst
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Role details
Tech stack
Job 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.
Requirements
- 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.
About the company
At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job-you will find purpose and pride., We foster continuous learning: Build expertise in algorithmic thinking, data analysis, pharmacovigilance systems, and global regulations while solving real-world challenges that matter.
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We challenge you to grow: You drive your career. We provide a stimulating environment, meaningful challenges, and opportunities that help you reach your full potential.
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We create career opportunities: Explore diverse career paths across PV Technology and the broader organization as your interests and expertise evolve.
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We support flexible working: Benefit from flexible working hours and home-office opportunities that help you balance professional and personal priorities.
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We provide global exposure: Collaborate with colleagues across Europe, Asia-Pacific, and the United States, gaining experience in a truly global organization.
Ready to Make a Global Impact?
Leverage your expertise. Drive innovation. Shape the future of pharmacovigilance data management. Join Baxter and make a difference for patients worldwide.
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Prepare application
- Draft this with your agent
- Open in Claude
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