Abbott in the United States is seeking a Senior Project Manager/Clinical Evaluations to support regulatory submissions for medical devices. This on-site role focuses on CER development, review, and regulatory strategy across EU MDR requirements, with cross-functional collaboration among R&D, Regulatory Affairs, and Quality teams.
The CER PM will lead writing and oversight of CERs, CEPs, PMCF plans, and related documents, ensuring safety and performance data support lifecycle evaluations.
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