Lisa Vershave is an accomplished regulatory affairs manager at Revvity, with a robust background in clinical study management and research. With experience at PerkinElmer, Inc. as a clinical study manager and at Eli Lilly and Company as a clinical trial project manager, Lisa has demonstrated expertise in overseeing clinical trials. Prior roles at Roche and Covance involved significant responsibilities in clinical research and investigator training. Lisa began a career in medical technology, serving as a medical technologist where skills in clinical chemistry testing were developed. Lisa holds a Bachelor of Science in Medical Technology from Michigan State University.
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