Danielle Phillips is a seasoned professional with extensive experience in regulatory data management and document control within the pharmaceutical industry. Notably, Danielle has held positions at Merck, including Regulatory Data Coordinator and roles in the Merck Regulatory Submissions Group, where the focus was on processing data/system issues for global product registration databases. Additional experience includes serving as a Document Control Specialist at Axelon Services Corp./Johnson & Johnson and Document Control Administrator II at Yoh, where responsibilities involved technical specifications and electronic document systems. Prior roles also include management and administrative positions at Fossil and Medarex, Inc., complemented by a solid educational background in Computer Information Systems and Psychology from High Point University and Kaplan University, respectively.
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