A leading global healthcare company is seeking a Senior Manager in Regulatory Affairs to develop and execute submission plans for regulatory submissions. This role requires strong project management skills, along with a Bachelor's degree in a relevant field and over 5 years of experience in the pharma or biotech industries. The successful candidate will collaborate with cross-functional teams and ensure compliance with global regulatory guidelines. The position is based in Raleigh, NC, with an onsite requirement of 3 days a week.
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