Jennifer T. is an experienced Regulatory Affairs Program Manager currently employed at Abbott since June 2022. Prior to this role, Jennifer worked at Medtronic, serving as the Principal China Clinical Evaluation Specialist, where responsibilities included authoring multiple China Clinical Evaluation Reports (CERs) and leading a working group for procedure harmonization. As a China Program Manager, Jennifer successfully managed submission activities and achieved the registration of 10 products in nine months. In earlier roles at Medtronic Structured Heart and Medtronic Inc., Jennifer contributed to global regulatory submissions, developed marketing claims, and provided regulatory support across various functions. Jennifer holds a Master's degree in Pharmaceutical Sciences from the University of Cincinnati.
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