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Job Description & How to Apply Below
IQVIA is seeking a Regulatory Program Manager in Reading, UK, to support regulatory processes throughout drug development and submission phases. You will provide project management, maintain regulatory schedules, and collaborate cross-functionally to ensure successful global filings.
The ideal candidate holds a B.S. in pharmaceutical-related subjects and possesses 5 years of relevant experience in regulatory affairs and project management. Strong skills in project planning and risk management are essential for this role.
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