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Bristol Myers Squibb is seeking a regulatory documents professional to coordinate and author essential submissions and regulatory documents across drug development programs. You will integrate scientific, medical, and regulatory input from cross-functional teams to accelerate submissions and
Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
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