Senior Specialist, Submission Management
Bristol Myers Squibb · Warsaw, Poland
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Role summary
This senior specialist role manages investigational and global regulatory submissions across Bristol Myers Squibb's international teams. The position involves coordinating dossier development, overseeing eCTD publishing, and tracking submission timelines to ensure compliance and on-time delivery to health authorities. The candidate should have 1–3+ years of regulatory submission experience, familiarity with submission tools, and demonstrated ability to work effectively in global, cross-functional environments.
Privacy & handoff
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