Senior Regulatory Affairs & Medical Writing Specialist

Bristol Myers Squibb, Princeton, NJ, is seeking a Regulatory Affairs/Medical Writing professional to coordinate and author complex regulatory documents for submissions worldwide. The role integrates scientific, medical, and regulatory input from development teams for immunology and cardiovascular assets.
The candidate will ensure adherence to global documentation standards, manage timelines, and lead teams to deliver high-quality CTD summaries and related materials for regulatory agencies.

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