John Kremer

Background

About John Kremer

Over 14 years of experience as a manager, cardiac safety scientist, or study director for nonclinical safety assessment studies. Author of more than 700 reports that have been fully accepted by worldwide regulatory agencies. Effective champion of process improvements/automation projects to expedite data analysis, compilation, and reporting as well as a Subject Matter Expert for SEND datasets for nonclinical cardiovascular endpoints. Experienced manager whose team of highly skilled scientists supports toxicology and pharmacology studies across global sites. Skilled scientific communicator with many presentations and publications: Author/co-author of 12 peer-reviewed publications; lead author on 13 presentations or posters at national meetings (plus more as a co-author); and chairperson of 2 sessions at the National Society of Toxicology meeting. More than 2 years of experience in the medical device industry developing combination drug/device products to treat cardiac atherosclerosis.