Though Elsevier is best known for a storied history in scholarly publishing, we have evolved our business into a decision support and analytics powerhouse that serves the needs of clinicians and scientists. Among our leading products are clinical pathways tools that guide clinicians in the dissemination of evidence based care. Based on evolving medical device regulations, these sophisticated software solutions, which aim to “improve every patient outcome,” are increasingly likely to be classified as “Software as a Medical Device” (SaMD). Thus, Elsevier has begun its journey into the world of regulated products and is seeking seasoned quality and regulatory professionals to join the team. Job Function: Leads the establishment and implementation
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