6 дней назад
Senior Global Pharmacovigilance Data Analyst (SQL)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Global Pharmacovigilance Data Analyst (SQL): Developing, validating, and optimizing reporting solutions and SQL queries for critical pharmacovigilance data with an accent on data integrity, reporting quality, and global stakeholder collaboration. Focus on investigating complex data issues, conducting root cause analyses, automating reporting processes, and supporting safety-system enhancements.
Location: Vienna, Austria; Warsaw, Poland; or Malta. Flexible working hours and home-office opportunities are available.
Company
Global healthcare company focused on developing solutions that support patient safety and improve healthcare delivery.
What you will do
- Lead the development, validation, and optimization of complex pharmacovigilance reporting solutions and SQL queries.
- Generate and oversee critical periodic and ad hoc safety reports.
- Investigate data integrity and reporting issues, perform root cause analyses, and drive corrective actions.
- Partner with IT, Safety Systems, Regulatory Affairs, Medical Affairs, and other global functions.
- Identify automation and process-improvement opportunities and support system enhancements, testing, and implementation projects.
- Mentor junior team members and share reporting and data-management best practices.
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.
- Ability to translate business requirements into scalable reporting solutions.
- Excellent stakeholder-management and communication skills in complex global and cross-functional environments.
Nice to have
- Experience with pharmacovigilance systems such as Argus or ARISg.
- Experience with Cognos or comparable reporting platforms.
- Background in pharmacovigilance, drug safety, or clinical data management.
- Experience with reporting automation and process-improvement initiatives.
Culture & Benefits
- Flexible working hours and home-office opportunities.
- Continuous learning in algorithmic thinking, data analysis, pharmacovigilance systems, and global regulations.
- Career-development opportunities across PV Technology and the broader organization.
- Collaboration with colleagues across Europe, Asia-Pacific, and the United States.
- Work on data-management challenges that support patient safety worldwide.
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